Generated by All in One SEO v4.9.10, this is an llms.txt file, used by LLMs to index the site. # PVpharm Pharmaceutical services for the Pharmaceutical Industry. ## Sitemaps - [XML Sitemap](https://pvpharm.com/sitemap.xml): Contains all public & indexable URLs for this website. ## Posts - [News](https://pvpharm.com/news/) - July 1, 2026 PVpharm participará en el IV Congreso Peruano de Farmacovigilancia y... PVpharm participará en el IV Congreso Peruano de Farmacovigilancia y Tecnovigilancia 2026 en Lima July 1, 2026 PVpharm will participate in the 42nd Pharmacovigilance India 2026, taking... PVpharm at the 42nd Pharmacovigilance India 2026 June 29, 2026 PVpharm is leading the way - [PVpharm participará en el IV Congreso Peruano de Farmacovigilancia y Tecnovigilancia 2026 en Lima](https://pvpharm.com/pvpharm-participara-en-el-iv-congreso-peruano-de-farmacovigilancia-y-tecnovigilancia-2026-en-lima/) - PVpharm participará en el IV Congreso Peruano de Farmacovigilancia y Tecnovigilancia 2026 en Lima, con ponencias sobre IA, gestión de riesgos, auditorías e inspecciones en farmacovigilancia. - [PVpharm at the 42nd Pharmacovigilance India 2026](https://pvpharm.com/pvpharm-at-the-42nd-pharmacovigilance-india-2026/) - PVpharm CEO Jose Alberto Ayala Ortiz will join Pharmacovigilance India 2026 in Hyderabad to discuss the future of pharmacovigilance outsourcing. - [Pharmacovigilance training VII edition, Barcelona & Online 12-13 May 2026 - Video and evaluation](https://pvpharm.com/pharmacovigilance-training-vii-edition-barcelona-online-12-13-may-2026-video-and-evaluation/) - PVpharm is leading the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. - [PVpharm Proudly Participates as Silver Sponsor at the 43rd AEFI Symposium in Barcelona](https://pvpharm.com/pvpharm-proudly-participates-as-silver-sponsor-at-the-43rd-aefi-symposium-in-barcelona/) - PVpharm was delighted to participate as a Silver Sponsor of the 43rd AEFI Symposium, one of Spain's leading scientific meetings for professionals working in the pharmaceutical industry, held this year in Barcelona. The symposium once again brought together experts from across the pharmaceutical sector, regulatory authorities, academia, and healthcare organizations to discuss the latest developments PVpharm proudly participated as Silver Sponsor at the 43rd AEFI Symposium in Barcelona, strengthening its commitment to innovation and excellence in pharmacovigilance. - [Online EVWeb training for SPONSORS 5-6 May 2026](https://pvpharm.com/online-evweb-training-for-sponsors-5-6-may-2026/) - José Ortiz, CEO of PVpharm will be participating as a trainer, in the next EVWeb training specifically targeted for SPONSORs of Clinical trials on 5-6 May 2026. The training will be delivered online in the evening time (14:00-15:00 CET). The training is targeted to: -Sponsors who have to report and analyse suspected adverse reactions in - [Training Online XEVMPD for SPONSORS 28-29 Apr 2026](https://pvpharm.com/training-online-xevmpd-for-sponsors-28-29-apr-2026/) - This training will focus on explaining the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM) and the use of the XEVMPD data entry tool (EVWEB). - [III Jornadas Universitarias de Farmacovigilancia Universidad de Granada, 26-27 mayo 2026](https://pvpharm.com/iii-jornadas-universitarias-de-farmacovigilancia-universidad-de-granada-26-27-mayo-2026/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada, tienen el placer de invitarles a participar en las III Jornadas de Farmacovigilancia Universidad de Granada, los días 26 y 27 de mayo (martes y miércoles) de 2026, a partir de las 16:00 horas hasta las 18:30 hora española (para - [1ª Jornadas de Farmacovigilancia Universidad de Granada](https://pvpharm.com/1a-jornadas-de-farmacovigilancia-universidad-de-granada/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada, tienen el placer de invitarles a participar en las 1ª Jornadas de Farmacovigilancia Universidad de Granada, que se celebrará los próximos días 5 y 6 de junio (miércoles y jueves) de 2024, a partir de las 16:00 horas hasta las - [2ª Jornadas Universitarias de Farmacovigilancia Universidad de Granada, 21-22 mayo 2025](https://pvpharm.com/2a-jornadas-universitarias-de-farmacovigilancia-universidad-de-granada-21-22-mayo-2025/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada, tienen el placer de invitarles a participar en las 2ª Jornadas de Farmacovigilancia Universidad de Granada, los días 21 y 22 de mayo (miércoles y jueves) de 2025, a partir de las 16:00 horas hasta las 18:30 hora española. Posteriormente - [EMA PMS Deadlines: MAHs to act as soon as possible!](https://pvpharm.com/ema-pms-deadlines-mahs-to-act-as-soon-as-possible/) - The EMA PMS is driving strict timelines for MAHs to submit structured product data. Companies can be supported in this activity by PVpharm. Regulatory Timelines: Clear Deadlines, Limited Time The EMA has defined a phased roadmap for PMS data submission. Key milestones: June 2026: enrichment of manufacturer data and pack sizes for critical medicines December - [PVpharm Participates in the “Diploma in Applications of Pharmacovigilance” at the University of Panama](https://pvpharm.com/pvpharm-participates-in-the-diploma-in-applications-of-pharmacovigilance-at-the-university-of-panama/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the "1st Peruan Congress" carried out by the Peruvian Society of Pharmacovigilance. - [PVpharm reafirma su compromiso con el talento científico y la seguridad del paciente como patrocinador de la XVI Reunión de Jóvenes Farmacólogos de Andalucía (RJOFA) 2026](https://pvpharm.com/pvpharm-reafirma-su-compromiso-con-el-talento-cientifico-y-la-seguridad-del-paciente-como-patrocinador-de-la-xvi-reunion-de-jovenes-farmacologos-de-andalucia-rjofa-2026/) - España, 6 de mayo de 2026 – PVpharm, consultora líder internacional especializada en servicios integrales de farmacovigilancia, anuncia con gran entusiasmo su participación como patrocinador oficial de la XVI edición de la Reunión de Jóvenes Farmacólogos de Andalucía (RJOFA), el destacado encuentro científico que tendrá lugar el próximo 26 de junio de 2026. Con este patrocinio, PVpharm da un paso más - [Conoce PVpharm! Visita nuestro stand en la Feria de Empleo 2026 en la Universidad de Almería](https://pvpharm.com/conoce-pvpharm-visita-nuestro-stand-en-la-feria-de-empleo-2026-en-la-universidad-de-almeria/) - PVpharm will be participating in the “Feria de Empleo 2026”, along with other companies and organizations from Almería like Cosentino, Cajamar, and many others!. This job fair dedicates two days in which local companies have the opportunity to make themselves known in a closer way and thus create a common space where both, the student - [Navigating the AI Revolution in Pharmacovigilance: Insights from the CIOMS WG XIV Report](https://pvpharm.com/navigating-the-ai-revolution-in-pharmacovigilance-insights-from-the-cioms-wg-xiv-report/) - See the full video of the presentation by José Ortiz to the Peruvian Society of Pharmacovigilance below (Spanish) On Saturday 21st March 2026, José Ortiz was invited by the Peruvian Society of Pharmacovigilance (SOPEFAR) to talk about the CIOMS Working Group XIV Report. Please see the video in Spanish below, summary in English follow below. - [𝗜𝗻𝘁𝗲𝗹𝗶𝗴𝗲𝗻𝗰𝗶𝗮 𝗔𝗿𝘁𝗶𝗳𝗶𝗰𝗶𝗮𝗹 𝗲𝗻 𝗙𝗮𝗿𝗺𝗮𝗰𝗼𝘃𝗶𝗴𝗶𝗹𝗮𝗻𝗰𝗶𝗮 - 𝗘𝗻𝗳𝗼𝗾𝘂𝗲 𝗘𝘀𝘁𝗿𝗮𝘁é𝗴𝗶𝗰𝗼 𝗯𝗮𝗷𝗼 𝗹𝗮𝘀 𝗥𝗲𝗰𝗼𝗺𝗲𝗻𝗱𝗮𝗰𝗶𝗼𝗻𝗲𝘀 𝗱𝗲 𝗖𝗜𝗢𝗠𝗦](https://pvpharm.com/𝗜𝗻𝘁𝗲𝗹𝗶𝗴𝗲𝗻𝗰𝗶𝗮-𝗔𝗿𝘁𝗶/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the "1st Peruan Congress" carried out by the Peruvian Society of Pharmacovigilance. - [PVpharm at DIA Europe Annual Meeting 2026, booth H11](https://pvpharm.com/pvpharm-at-dia-europe-annual-meeting-2026-booth-h11/) - PVpharm is pleased to announce the participation in the DIA Europe Annual Meeting 2026, taking place on March 24-26, 2026. This important event brings together professionals from across the globe to discuss the latest developments in pharmacovigilance, regulatory science, and patient safety. DIA’s European regional annual meeting - the largest neutral conference in the European - [Online XEVMPD training 11-13 March 2026](https://pvpharm.com/online-xevmpd-training-11-13-march-2026/) - José Alberto Ayala Ortiz and Monika Gappa from PVpharm, will be participating as trainers in the next XEVMPD training on 11-13 March 2026. The training will be delivered online in the morning time (09:00-13:00 CET). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information - [Faculty at Signal Management training by DIA March 2026](https://pvpharm.com/faculty-at-signal-management-training-by-dia-march-2026/) - On 3-6 March 2026, José Ortiz provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated data mining techniques. • Design - [Microcredencial de Farmacovigilancia de la Universidad de Granada - 2026](https://pvpharm.com/microcredencial-de-farmacovigilancia-de-la-universidad-de-granada-2026/) - PVpharm tiene el honor de anunciar la segunda edición de la Microcredencial de Farmacovigilancia de la Universidad de Granada. La Microcredencial ha sido desarrollada dentro del marco de actividades del Aula de Farmacovigilancia PVpharm UGR, y está diseñada para abordar de manera práctica todos los aspectos relevantes de la gestión de la seguridad de los - [Online EVWeb training 26-30 January 2026](https://pvpharm.com/online-evweb-training-26-30-january-2026/) - José Ortiz from PVpharm will be participating as a trainer, in the next EVWeb training on 26-30 January 2026. The training will be delivered online in the morning time (9:00-13:30 CET). The training is targeted to: -Users who have to report and analyse suspected adverse reactions in the pre- and post-authorisation phase using the ISO/ICH - [DIA Pharmacovigilance QMS virtual course (22 - 25 September 2025)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-22-25-september-2025/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 13:00 to 17:30 (CEST) between the 22nd and the 25th of September, 2025. The course will employ a mix of informative sessions, real case studies, and - [PVpharm Expands Its Services to Include Environmental Risk Assessments (ERA) for Medicinal Products](https://pvpharm.com/pvpharm-expands-its-services-to-include-environmental-risk-assessments-era-for-medicinal-products/) - PVpharm is pleased to announce the expansion of its regulatory and scientific services to include Environmental Risk Assessments (ERA) for medicinal products. This new service strengthens our commitment to sustainable and responsible pharmaceutical development, supporting our clients in meeting European and international regulatory requirements. Legislation and Context In the European Union, conducting an ERA is - [PVpharm participates in World Diabetes Day 2025 at the University of Almería ](https://pvpharm.com/pvpharm-participates-in-world-diabetes-day-2025-at-the-university-of-almeria/) - PVpharm is proud to announce its participation in the World Diabetes Day 2025 event organized by the Faculty of Health Sciences at the University of Almería (UAL). This initiative forms part of the global campaign led by the International Diabetes Federation (IDF) to raise awareness and promote education about diabetes prevention and management. The event - [Comply with the mandatory use of EVDAS for Signal Detection](https://pvpharm.com/comply-with-the-mandatory-use-of-evdas-for-signal-detection/) - On 22 July 2025, the Commission Implementing Regulation (EU) 2025/1466 was issued, coming into effect on 12 August 2025. This new regulation introduces significant updates to the European pharmacovigilance framework, particularly in relation to signal management processes.One of the main changes is the mandatory use of the EudraVigilance Data Analysis System (EVDAS) as a source for signal detection, in - [PVpharm at the European Pharmacovigilance Congress 2025 – See You in Milan!](https://pvpharm.com/pvpharm-at-the-european-pharmacovigilance-congress-2025-see-you-in-milan/) - Next November 28, 2025, PVpharm will be attending the European Pharmacovigilance Congress 2025, taking place in Milan. About the Congress The European Pharmacovigilance Congress is one of the leading scientific forums in Europe dedicated to drug safety. Known for its scientific depth, rich discussions, and international participation, the event brings together experts, regulators, and industry - [PVpharm at the World Drug Safety Congress Americas 2025 – Meet Us at Stand 637](https://pvpharm.com/pvpharm-at-the-world-drug-safety-congress-americas-2025-meet-us-at-stand-637/) - We are pleased to announce that PVpharm will be participating in the World Drug Safety Congress Americas 2025, taking place on November 4–6 in Boston, USA. About the Congress This premier event will convene over 1,500 global experts to address the most pressing challenges in drug safety and explore the transformative potential of technologies such - [Acto de presentación de actividades del Aula de Farmacovigilancia PVpharm - UGR - Curso 2025/26 - Congreso CONESFAR](https://pvpharm.com/acto-de-presentacion-de-actividades-del-aula-de-farmacovigilancia-pvpharm-ugr-curso-2025-26-congreso-conesfar/) - El Viernes 17-10-2025, entre las 12:00-13:30 CEST, dentro del marco del Congreso CONESFAR tendrá lugar en el Aula Magna de la Facultad de Farmacia de la Universidad de Granada, la presentación de actividades del Aula de Farmacovigilancia UGR & PVPharm para el curso 2025/26. ¿Por qué asistir?Durante la presentación, conocerán en detalle las actividades y oportunidades - [DIA Pharmacovigilance System Master File (PSMF) virtual course (28-29 October 2025)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-virtual-course-28-29-october-2025/) - José Ortiz will be participating as a trainer together with Marcela Fialova and Helen Emery, Pharmacovigilance Inspector at the Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom in the Pharmacovigilance System Master File (PSMF) course organized by DIA. The training will be delivered online from 1:00 PM to 5:00 PM (CET) on November 28 - [Online XEVMPD training 20-22 October 2025](https://pvpharm.com/online-xevmpd-training-20-22-october-2025/) - José Alberto Ayala Ortiz and Monika Gappa from PVpharm, will be participating as trainers in the next XEVMPD training on 20-22 October 2025. The training will be delivered online in the morning time (09:00-13:00 CET). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information - [Online EVWeb training 13-17 October 2025](https://pvpharm.com/online-evweb-training-13-17-october-2025/) - José Ortiz and Monika Gappa from PVpharm will be participating as a trainer, in the next EVWeb training on 13-17 October 2025. The training will be delivered online in the afternoon time (13:00-17:00 CET). The training is targeted to: -Users who have to report and analyse suspected adverse reactions in the pre- and post-authorisation phase - [Meet us at ISoP Annual Meeting in El Cairo 2025](https://pvpharm.com/meet-us-at-isop-annual-meeting-in-el-cairo-2025/) - PVpharm is going to present a poster communication at ISoP 24rd annual meeting in El Cairo, October 24-27 2025. The International Society of Pharmacovigilance (ISoP) is a professional, independent and a non-profit society for promoting the safe and effective use of medicinal products. ISoP’s main aim is ‘to foster science and learning in pharmacovigilance in - [PVpharm at the World Drug Safety Congress Europe 2025 – Meet Us at Stand 48!](https://pvpharm.com/pvpharm-at-the-world-drug-safety-congress-europe-2025-meet-us-at-stand-48/) - We are pleased to announce that PVpharm will be participating in the World Drug Safety Congress Europe 2025, taking place on October 7–8 in Amsterdam, Netherlands. About the Congress This premier event will convene over 1,500 global experts to address the most pressing challenges in drug safety and explore the transformative potential of technologies such - [PVpharm participates in the IV Pharmaceutical Law Congress at ICAM](https://pvpharm.com/pvpharm-participates-in-the-iv-pharmaceutical-law-congress-at-icam/) - PVpharm is happy to announce the participation of Mayte Alonso, Head of Operations at PVpharm, in the upcoming IV Pharmaceutical Law Congress organized by the Pharmaceutical Law Section of the Madrid Bar Association (ICAM). The event will take place on September 18 and 19, 2025, at ICAM’s headquarters on Calle Serrano in Madrid. This prestigious - [PVpharm at DIA India Annual Meeting 2025](https://pvpharm.com/pvpharm-at-dia-india-annual-meeting-2025/) - PVpharm is pleased to announce the participation of Jose Alberto Ayala Ortiz, PVpharm CEO, as a speaker in the upcoming the DIA India Annual Meeting 2025, taking place at the NESCO Center in Mumbai on September 19, 2025. This important event brings together professionals from across the globe to discuss the latest developments in pharmacovigilance, - [PVpharm at Farmaforum 2025 in IFEMA Madrid](https://pvpharm.com/pvpharm-at-farmaforum-2025-in-ifema-madrid/) - On September 17–18, 2025, PVpharm will proudly participate once again in Farmaforum, Spain’s premier event for the pharmaceutical industry, held at IFEMA Madrid. About Farmaforum 2025 The 11th edition of Farmaforum – Forum of the Pharmaceutical, Biopharmaceutical, and Laboratory Technologies Industry – will once again take place in Madrid. Over the years, Farmaforum has established - [DIA QPPV Talks Webinar: The Future of the QPPV Role in the Age of AI](https://pvpharm.com/dia-qppv-talks-webinar-the-future-of-the-qppv-role-in-the-age-of-ai/) - On 16 September 2025, pharmacovigilance professionals around the world will gather virtually for a unique opportunity to reflect on the future of the Qualified Person for Pharmacovigilance (QPPV) role. Hosted under the DIA QPPV Talks series, this free webinar will explore how artificial intelligence is reshaping regulatory practices and what it means for QPPVs, local - [ISO 9001:2015 Certification](https://pvpharm.com/iso-90012015-certification/) - PVpharm Achieves ISO 9001:2015 Certification, Marking a Major Milestone in Quality and Excellence PVpharm is proud to announce that it has officially obtained ISO 9001:2015 certification, a globally recognized standard for quality management systems. This achievement underscores PVpharm's unwavering commitment to excellence, precision, and continuous improvement in all aspects of its operations. The ISO 9001:2015 - [Mayte Alonso joins PVpharm as Head of Operations to support international growth](https://pvpharm.com/mayte-alonso-joins-pvpharm-as-head-of-operations-to-support-international-growth/) - Mayte Alonso’s arrival at PVpharm reinforces the company’s commitment to expanding its presence in the global pharmaceutical services market. PVpharm is pleased to announce that Mayte Alonso has joined the company as a strategic addition to its team, strengthening its capabilities in pharmacovigilance, medical information, and regulatory consulting services across international markets.Mayte brings a robust - [ASEBIO, Colegio de Farmacéuticos de Granada and other sources are publishing about the 2ª Jornadas Universitarias de Farmacovigilancia Universidad de Granada, 21-22 mayo 2025](https://pvpharm.com/asebio-colegio-de-farmaceuticos-de-granada-and-other-sources-are-publishing-about-the-2a-jornadas-universitarias-de-farmacovigilancia-universidad-de-granada-21-22-mayo-2025/) - Los días 21 y 22 de mayo de 2025 se celebraron las II Jornadas Universitarias de Farmacovigilancia e Industria Farmacéutica organizadas por el Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada. Estas jornadas fueron la oportunidad para un encuentro entre profesionales del sector farmacéutico y estudiantes universitarios, que se - [Pharmacovigilance training VI edition, Barcelona & Online 12-13 May 2025 - Follow up with video and evaluation](https://pvpharm.com/pharmacovigilance-training-vi-edition-barcelona-online-12-13-may-2025-follow-up-with-video-and-evaluation/) - PVpharm is leading the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. - [Mandatory Use of OMS for National Marketing Authorization Applications – Is your company ready?](https://pvpharm.com/mandatory-use-of-oms-for-national-marketing-authorization-applications-is-your-company-ready/) - The Spanish Agency of Medicines and Health Products (AEMPS) has announced a major regulatory update: starting July 1, 2025, the Organization Management Service (OMS) will be mandatory for all new marketing authorization applications and variations processed through the national procedure. What does change with this new requirement?• The use of OMS will be compulsory for - [International PV requirements and training in Pharmacovigilance - VIDEO](https://pvpharm.com/international-pv-requirements-and-training-in-pharmacovigilance-video/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the "1st Peruan Congress" carried out by the Peruvian Society of Pharmacovigilance. - [DIA Pharmacovigilance System Master File (PSMF) and Global PSMF virtual courses (1-2 and 3 April 2025)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-and-global-psmf-virtual-courses-1-2-and-3-april-2025/) - José Ortiz will be participating as a trainer together with Marcela Fialova and Silvia Danesi in the Pharmacovigilance System Master File (PSMF) and Global PSMF courses organized by DIA. The training will be delivered online from 9:00 to 13:00 (CET) on April 1-2 and 3, 2025. These virtual live training courses covers essential concepts and - [Pharmacovigilance training VI edition, Barcelona & Online 12-13 May 2025](https://pvpharm.com/pharmacovigilance-training-vi-edition-barcelona-online-12-13-may-2025/) - PVpharm is leading the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. - [Visita nuestro stand en la Feria de Empleo 2025 en la Universidad de Almería](https://pvpharm.com/visita-nuestro-stand-en-la-feria-de-empleo-2025-en-la-universidad-de-almeria/) - PVpharm will be participating in the “Feria de Empleo 2025”, along with other companies and organizations from Almería like Cosentino, Cajamar, and many others!. This job fair dedicates two days in which local companies have the opportunity to make themselves known in a closer way and thus create a common space where both, the student - [International PV requirements and training in Pharmacovigilance](https://pvpharm.com/international-pv-requirements-and-training-in-pharmacovigilance/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the "1st Peruan Congress" carried out by the Peruvian Society of Pharmacovigilance. - [PVpharm in the 1st Peruvian Congress on Pharmacovigilance](https://pvpharm.com/pvpharm-in-the-1st-peruvian-congress-on-pharmacovigilance/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the "1st Peruan Congress" carried out by the Peruvian Society of Pharmacovigilance. - [Meet us in Basel at DIA EU 2025!](https://pvpharm.com/meet-us-in-basel-at-dia-eu-2025/) - PVpharm is participating in the DIA Europe conference 2025. Meet us at Stand C-9! DIA’s European regional annual meeting is the largest neutral conference in the European life sciences arena for the last 37 years!As the knowledge and innovation hub uniting science, healthcare, patients and regulatory professionals, DIA Europe 2025 commits to transforming insights into - [Clinical Trials Information System (CTIS) training 25-28 March 2025](https://pvpharm.com/clinical-trials-information-system-ctis-training-25-28-march-2025/) - The European Commission has informed that the entry into application of the Clinical Trials Regulation (CTR) - [Faculty at Signal Management training by DIA March 2025](https://pvpharm.com/faculty-at-signal-management-training-by-dia-march-2025/) - On 4-7 March 2025, José Ortiz provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated data mining techniques. • Design - [Nueva Microcredencial de Farmacovigilancia de la Universidad de Granada](https://pvpharm.com/nueva-microcredencial-de-farmacovigilancia-de-la-universidad-de-granada/) - PVpharm tiene el honor de anunciar la creación de la nueva Microcredencial de Farmacovigilancia de la Universidad de Granada. La Microcredencial ha sido desarrollada dentro del marco de actividades del Aula de Farmacovigilancia PVpharm UGR, y está diseñada para abordar de manera práctica todos los aspectos relevantes de la gestión de la seguridad de los - [¡Tenemos ganador del Premio del AulaFV!](https://pvpharm.com/tenemos-ganador-del-premio-del-aulafv/) - PVpharm, en colaboración con la Facultad de Farmacia de la Universidad de Granada, tiene el placer de anunciar el ganador de la Primera Edición del Premio Aula de FV-UGR, que ha sido D. Alejandro Ruiz Malagón. El premio fué entregado en los actos conmemorativos en honor a nuestra patrona, la Inmaculada Concepción, el domingo, 1 - [PVpharm at Upcoming EVWeb Training – This December!](https://pvpharm.com/pvpharm-at-upcoming-evweb-training-this-december/) - José Ortiz, CEO of PVpharm, will be participating as a trainer in the upcoming EVWeb training, scheduled from Monday, 02 December to Friday, 06 December 2024. This comprehensive online training will take place all day and is tailored for professionals involved in reporting and analyzing suspected adverse reactions. About the Training EudraVigilance is the EU's - [European Pharmacovigilance Congress For Year 2024: The Key Takeaways and PVpharm’s Participation](https://pvpharm.com/european-pharmacovigilance-congress-for-year-2024-the-key-takeaways-and-pvpharms-participation/) - The European Pharmacovigilance (EUPV) Congress 2024, held both virtually and in-person in Milan, Italy, once again demonstrated why it is a premier event for pharmacovigilance professionals worldwide. Organized by the Pharma Education Center, the congress brought together leading minds to explore emerging trends, share scientific advancements, and discuss strategies to enhance drug safety practices globally. - [A Milestone Partnership: PVpharm & Teófilo Hernando Institute](https://pvpharm.com/a-milestone-partnership-pvpharm-teofilo-hernando-institute/) - At PVpharm, we are excited to celebrate another key milestone in our journey as we announce our collaboration with the Teófilo Hernando Foundation Institute (ITH). This partnership marks a significant step forward in our commitment to advancing pharmacovigilance and clinical safety services, while also supporting cutting-edge research in drug development and innovation. The Teófilo Hernando - [Breakthrough Highlights From The 2024 National Pharmacovigilance Conference, First Prize of the Poster Category](https://pvpharm.com/breakthrough-highlights-from-the-2024-national-pharmacovigilance-conference-first-price-of-the-poster-category/) - The National Pharmacovigilance Conference is an annual event that brings together experts to discuss the latest developments in drug safety and pharmacovigilance. This year’s event, held in Oviedo, Spain, offered valuable insights on topics such as artificial intelligence in healthcare, innovative reporting methods, and the growing importance of communication in pharmacovigilance. PVpharm was proud to - [PVpharm Sponsors The 76th CREUP Assembly: This Year In Granada](https://pvpharm.com/pvpharm-sponsors-the-76th-creup-assembly-this-year-in-granada/) - We are thrilled to announce that PVpharm will be sponsoring the 76th Assembly of CREUP (La Coordinadora de Representantes de Estudiantes de Universidades Públicas), which will take place in the vibrant city of Granada from November 20th to 24th, 2024. CREUP is a leading organization representing over 1,000,000 students across 37 public universities in Spain. - [Lecturer at the Global Pharmacovigilance Congress - Global PV Society](https://pvpharm.com/lecturer-at-the-global-pharmacovigilance-congress-global-pv-society/) - José Ortiz will be one of the speakers at the International Pharmaceutical Industry Congress - Latin America 2021. This is the most important event of the Pharmaceutical Industry in the region. - [DIA Pharmacovigilance System Master File (PSMF) and Global PSMF virtual courses (26-27 and 28 November 2024)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-and-global-psmf-virtual-courses-26-27-and-28-november-2024/) - José Ortiz will be participating as a trainer together with Marcela Fialova and Silvia Danesi in the Pharmacovigilance System Master File (PSMF) and Global PSMF courses organized by DIA. The training will be delivered online from 13:00 to 17:00 (CET) on November 27-28 and 29, 2024. These virtual live training courses covers essential concepts and - [Faculty at Signal Management training by DIA November 2024](https://pvpharm.com/faculty-at-signal-management-training-by-dia-november-2024/) - On 18-21 November 2024, José Ortiz provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated data mining techniques. • Design - [PVpharm participará en las XIII Jornadas Nacionales de Farmacovigilancia](https://pvpharm.com/pvpharm-participara-en-las-xiii-jornadas-nacionales-de-farmacovigilancia/) - PVpharm participará en las XIII Jornadas Nacionales de Farmacovigilancia que tendrán lugar el 12 y 13 de Noviembre de 2024 en Oviedo, Asturias. PVpharm presentará el Aula de Farmacovigilancia PVpharm, una iniciativa conjunta con la Facultad de Farmacia de la Universidad de Granada, mediante una comunicación en forma de poster. Además, PVpharm contará con un - [Acto de presentación de actividades del Aula de Farmacovigilancia PVpharm - UGR - Curso 2024/25](https://pvpharm.com/acto-de-presentacion-de-actividades-del-aula-de-farmacovigilancia-pvpharm-ugr-curso-2024-25/) - El Jueves 24-10-2024, entre las 12:30-14:00 CEST, tendrá lugar en el Aula Magna de la Facultad de Farmacia de la Universidad de Granada, la presentación de actividades del Aula de Farmacovigilancia UGR & PVPharm para el curso 2024/25. ¿Por qué asistir?Durante la presentación, conocerán en detalle las actividades y oportunidades que hemos preparado para este curso - [¡Gana el Premio PVpharm-UGR por tu TFG en Farmacovigilancia!](https://pvpharm.com/gana-el-premio-pvpharm-ugr-por-tu-tfg-en-farmacovigilancia/) - La Facultad de Farmacia de la Universidad de Granada se complace en anunciar la Primera Edición del Premio Aula de Farmacovigilancia PVpharm-UGR. Este premio busca reconocer la excelencia en los Trabajos Fin de Grado (TFG) relacionados con la farmacovigilancia. ¿Eres estudiante de farmacia y has realizado una investigación destacada en este campo? ¡Esta es tu - [Poster presentation of Aula de Farmacovigilancia at ISoP Annual Meeting in Montreal 2024](https://pvpharm.com/poster-presentation-of-aula-de-farmacovigilancia-at-isop-annual-meeting-in-montreal-2024/) - PVpharm presented a poster communication about the Aula de Farmacovigilancia PVpharm Universidad de Granada at ISoP 23rd annual meeting in Montreal, October 1-5 2024. See some images of the ISoP poster presentation. The International Society of Pharmacovigilance (ISoP) is a professional, independent and a non-profit society for promoting the safe and effective use of medicinal - [PVpharm Unveils a New Look: The Story Behind Our Logo Transformation](https://pvpharm.com/pvpharm-unveils-a-new-look-the-story-behind-our-logo-transformation/) - Last week, we gave a sneak peek at something exciting—a bold step in our company’s journey of growth and evolution. Today, we're thrilled to reveal the full story behind PVpharm's new logo, symbolizing the dynamic shift happening within our organization. This change isn’t just cosmetic; it reflects the core of who we are and where - [Meet us at ISoP Annual Meeting in Montreal 2024](https://pvpharm.com/meet-us-at-isop-annual-meeting-in-montreal-2024/) - PVpharm is going to present a poster communication at ISoP 23rd annual meeting in Montreal, October 1-5 2024. The International Society of Pharmacovigilance (ISoP) is a professional, independent and a non-profit society for promoting the safe and effective use of medicinal products. ISoP’s main aim is ‘to foster science and learning in pharmacovigilance in all - [Don’t Miss Out: Join PVpharm At The Exciting FarmaForum 2024!](https://pvpharm.com/dont-miss-out-join-pvpharm-at-the-exciting-farmaforum-2024/) - We're excited to announce that PVpharm will be attending Farmaforum 2024, Spain's premier pharmaceutical industry event. This year's event will take place on September 25th and 26th, we will be at Hall 9 booth G31 of IFEMA Madrid. Farmaforum is offering a unique platform for networking, learning, and discovering the latest trends in the pharma, - [PVpharm participates in the Wheel of Fortune: A Diabetes Challenge!](https://pvpharm.com/pvpharm-participates-in-the-2024-european-researchers-night-wheel-of-fortune/) - Are You Ready to Spin the Wheel of Diabetes with PVpharm? Join the University of Almería and PVpharm for a unique and engaging experience at the Wheel of Fortune: Diabetes Edition. This interactive game will teach you about diabetes, its complications, and how to prevent them. How does it work? Imagine a giant wheel divided - [PVpharm's Summer meeting 2024: Mission, Vision and Objectives (VIDEO)](https://pvpharm.com/pvpharms-summer-meeting-2024-mission-vision-and-objectives-video/) - PVpharm has enjoyed several sessions where the team has worked on the Mission, Vision and Values.. - [DIA Pharmacovigilance QMS virtual course (16 - 19 September 2024)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-16-19-september-2024/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 13:00 to 17:30 (CEST) between the 16th and the 19th of September, 2024. The course will employ a mix of informative sessions, real case studies, and - [AulaFV UGR - Publicación de los resúmenes de las I Jornadas Universitarias de Farmacovigilancia](https://pvpharm.com/aulafv-ugr-publicacion-de-los-resumenes-de-las-i-jornadas-universitarias-de-farmacovigilancia/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada celebraron las I Jornadas Universitarias de Farmacovigilancia e Industria Farmacéutica durante los días 5 y 6 de junio de 2024. Los resúmenes de las presentaciones de las jornadas están publicados en la revista Ars Pharmaceutica, Vol 65 (Suppl 2) de - [Programa Especializado Buenas Prácticas de Farmacovigilancia](https://pvpharm.com/programa-especializado-buenas-practicas-de-farmacovigilancia/) - José Ortiz will be one of the speakers at the International Pharmaceutical Industry Congress - Latin America 2021. This is the most important event of the Pharmaceutical Industry in the region. - [AulaFV UGR - Curso de Introducción a la FV, 1ª Ed - GRABACIONES](https://pvpharm.com/aulafv-ugr-curso-de-introduccion-a-la-fv-1a-ed-grabaciones/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada celebraron el curso de Introducción a la Farmacovigilancia (1ª Edición), durante los días 19 y 20 de marzo (martes y miércoles) de 2024. Las grabaciones del curso están disponibles, y se puede adquirir en este link: Grabaciones del Curso disponibles - [Elena Marín is nominated for the Influential Women of Almería awards!](https://pvpharm.com/elena-marin-is-nominated-for-the-influential-women-of-almeria-awards/) - Elena Marín Cassinello, PVpharm's head of Finance and HR, has been nominated for the Influential Women of Almería awards. The Influential Women of Almería platform was created to give impetus and visibility to female talent in the province of Almería in what they are experts in. It is a meeting point for talented women from - [Brochure available! Pharmacovigilance training V edition, Madrid & Online 27-28 May 2024](https://pvpharm.com/brochure-available-pharmacovigilance-training-v-edition-madrid-online-27-28-may-2024/) - PVpharm is leading the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. - [DIA Pharmacovigilance System Master File (PSMF) and Global PSMF virtual courses (16-17 and 18 April 2024)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-and-global-psmf-virtual-courses-16-17-and-18-april-2024/) - José Ortiz will be participating as a trainer together with Marcela Fialova and Zoe Hamill in the Pharmacovigilance System Master File (PSMF) and Global PSMF courses organized by DIA. The training will be delivered online from 9:00 to 13:00 (CEST) on April 17-18 and 19, 2024. These virtual live training courses covers essential concepts and - [Clinical Trials Information System (CTIS) training 8-11 April 2024](https://pvpharm.com/clinical-trials-information-system-ctis-training-8-11-april-2024/) - The European Commission has informed that the entry into application of the Clinical Trials Regulation (CTR) - [PVpharm participates in “Feria de Empleo 2024” at the University of Almería](https://pvpharm.com/pvpharm-participates-in-feria-de-empleo-2024-at-the-university-of-almeria/) - PVpharm will be participating in the “Feria de Empleo 2024”, along with other companies and organizations from Almería like Cosentino, Cajamar, Kimitec, FAAM or Verdiblanca. This job fair dedicates two days in which local companies have the opportunity to make themselves known in a closer way and thus create a common space where both, the - [PVpharm extends the collaboration with the International AIDS Vaccine Initiative (IAVI)](https://pvpharm.com/pvpharm-extends-the-collaboration-with-the-international-aids-vaccine-initiative-iavi/) - We are so excited to announce the extension of our collaboration agreement with the International AIDS Vaccine Initiative (IAVI) to provide pharmacovigilance and regulatory consulting. IAVI is a nonprofit scientific research organization that develops vaccines and antibodies for HIV, tuberculosis, emerging infectious diseases (including COVID-19), and other neglected diseases, with a clear commitment to develop affordable and accesible solutions to these - [Pharmacovigilance training V edition, Madrid & Online 27-28 May 2024](https://pvpharm.com/pharmacovigilance-training-v-edition-madrid-online-27-28-may-2024/) - PVpharm is leading the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. - [Isabella Palagiano to participate as speaker in the AEFI Safety in Clinical Trials Training](https://pvpharm.com/isabella-pallagiano-to-participate-as-speaker-in-the-aefi-safety-in-clinical-trials-training/) - We are happy to announce that Isabella Palagiano will be participating as speaker in the AEFI Safety in Clinical trials Training. The training will take place on 29th February and 5th March and will be held online, please find more information about the training in the link below: During the 29th, Isabella will be talking - [AulaFV UGR - Curso de Introducción a la Farmacovigilancia, 1ª Edición](https://pvpharm.com/aulafv-ugr-curso-de-introduccion-a-la-farmacovigilancia-1a-edicion/) - El Aula de Farmacovigilancia PVpharm y la Facultad de Farmacia de la Universidad de Granada tienen el placer de invitarles a participar en el curso de Introducción a la Farmacovigilancia (1ª Edición), que se celebrará los próximos días 19 y 20 de marzo (martes y miércoles) de 2024, a partir de las 16:30 horas hasta - [PVpharm in TV (Canal Sur 6th Feb 2024)](https://pvpharm.com/pvpharm-in-tv-canal-sur-6th-feb-2024/) - Canal Sur TV was at PVpharm's offices to make an interview. Please see the video here: - [Online EVWeb training 29 January-2 February 2024](https://pvpharm.com/online-evweb-training-29-january-2-february-2024/) - José Ortiz, CEO of PVpharm will be participating as a trainer, in the next EVWeb training on 29 Janyary 2 February 2024. The training will be delivered online in the morning time (9:00-13:30 CET). The training is targeted to: -Users who have to report and analyse suspected adverse reactions in the pre- and post-authorisation phase - [Defafios actuais de Farmacovigilancia](https://pvpharm.com/defafios-actuais-de-farmacovigilancia/) - José Alberto Ayala Ortiz, CEO of PVpharm participated in the 1st edition of the Conference organized by OWL Pharma, Desafios Actuais de Farmacovigilancia, held in Lisbon on the 22nd of November 2023. José provided insight about Signal Detection in Pharmacovigilance and the use of EVDAS. Please check OWL Pharma website for more information: https://www.owlpharma.pt/news/o-futuro-de-farmacovigilancia-1a-edicao-desafios-atuais-de-farmacovigilancia **PVpharm - [Online EVWeb training for SPONSORS 27-29 November 2023](https://pvpharm.com/online-evweb-training-for-sponsors-27-29-november-2023/) - José Ortiz, CEO of PVpharm will be participating as a trainer, in the next EVWeb training specifically targeted for SPONSORs of Clinical trials on 27-29 November 2023. The training will be delivered online in the morning time (9:00-13:00 CET). The training is targeted to: -Sponsors who have to report and analyse suspected adverse reactions in - [Online XEVMPD training 27-29 November 2023](https://pvpharm.com/online-xevmpd-training-27-29-november-2023/) - José Alberto Ayala Ortiz, CEO of PVpharm, will be participating as trainer in the next XEVMPD training on 21-23 February 2024. The training will be delivered online in the morning time (09:00-13:00 CET). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal - [Online XEVMPD training 21-23 February 2024](https://pvpharm.com/online-xevmpd-training-21-23-february-2024/) - José Alberto Ayala Ortiz, CEO of PVpharm, will be participating as trainer in the next XEVMPD training on 21-23 February 2024. The training will be delivered online in the morning time (09:00-13:00 CET). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal - [DIA Pharmacovigilance QMS virtual course (27 February-1 March 2024)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-27-february-1-march-2024/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 9:00 AM to 13:30 PM (CET) between the 27th of February and the 1st March, 2024. The course will employ a mix of informative sessions, real - [Code of ethics in the use of Artificial Intelligence](https://pvpharm.com/code-of-ethics-in-the-use-of-artificial-intelligence/) - At PVpharm, we aim to work with pharmaceutical, biotech, and MedTech companies, providing new ideas and making solutions that make health better for everyone. We believe that Artificial Intelligence (AI) can really change the way we do pharmacovigilance, improving our work every day. The large revolution in the implementation of tools that use AI in - [Lecturer at the International Pharma Industry Congress - LATAM 2023](https://pvpharm.com/lecturer-at-the-international-pharma-industry-congress-latam-2023/) - José Ortiz will be one of the speakers at the International Pharmaceutical Industry Congress - Latin America 2021. This is the most important event of the Pharmaceutical Industry in the region. - [Creación del Aula de Farmacovigilancia PVpharm - UGR](https://pvpharm.com/creacion-del-aula-de-farmacovigilancia-pvpharm-ugr/) - El martes 24-10-2023 tuvo lugar en el Rectorado de la Universidad, la firma Aula de Farmacovigilancia UGR & PVPharm, un espacio dedicado a incrementar el conocimiento y aprendizaje sobre Farmacovigilancia y la Industria Farmacéutica. Al acto de firma acudieron entre otros el Sr. Rector Magnífico de la Universidad, D. Pedro Mercado Pacheco, el CEO y fundador de - [José Alberto Ayala Ortiz to participate as speaker in the AEFI Pharmacovigilance in Social Networks Training](https://pvpharm.com/jose-alberto-ayala-ortiz-to-participate-as-speaker-in-the-aefi-pharmacovigilance-in-social-networks-training/) - We are happy to announce that José Alberto Ayala Ortiz, PVpharm's CEO will be participating as speaker in the AEFI Pharmacovigilance in Social Networks Training. The training will take place on Monday 6th November from 16:00 to 19:00, please find more information about the training in the link below: https://aefi.org/eventos/farmacovigilancia-en-la-era-digital/?mc_cid=ddb97c2046&mc_eid=54a2a50032 During the session, José will - [DIA Pharmacovigilance System Master File (PSMF) and Global PSMF virtual courses (30 October and 2-3 November 2023)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-and-global-psmf-virtual-courses-30-october-and-2-3-november-2023/) - José Ortiz will be participating as a trainer together with Marcela Fialova in the Pharmacovigilance System Master File (PSMF) and Global PSMF courses organized by DIA. The training will be delivered online from 13:00 PM to 17:00 PM (CET) on October 30 and November 2 to 3, 2023. These virtual live training courses covers essential - [PVpharm participates in the 2023 European Researchers’ Night](https://pvpharm.com/pvpharm-participates-in-the-2023-european-researchers-night/) - The European Researchers' Night is a Europe-wide public event, which displays the diversity of science and its impact on citizens' daily lives in fun, inspiring ways. This year, the event will take place in 26 countries on Friday 29 September 2022. The European Researchers' Night aims to: -bring research and researchers closer to the public-promote - [PVpharm and Azierta agrees on a strategic alliance in Pharmacovigilance](https://pvpharm.com/pvpharm-and-azierta-agrees-on-a-strategic-alliance-in-pharmacovigilance/) - PVpharm and Azierta agrees on a strategic alliance in the field of Pharmacovigilance. This alliance will make it possible to jointly design and commercialize advanced pharmacovigilance services both for the Spanish market and internationally. The alliance signed places both companies in a position of reference in the health consulting sector in the field of pharmacovigilance - [PVpharm's Summer meeting 2023: Artificial Intelligence (VIDEO)](https://pvpharm.com/pvpharms-summer-meeting-2023-artificial-intelligence-video/) - PVpharm has enjoyed several sessions where the team has enjoyed sailing on one of the most wonderful landscapes of Spain, the coast of Almeria. - [Pharmacovigilance Webinar - Audit and Inspection (8 September 2023)](https://pvpharm.com/pharmacovigilance-webinar-audit-and-inspection-8-september-2023/) - José Ortiz will be participating as a trainer together with other speakers in the Pharmacovigilance Webinar - Audit and Inspection organized by the Global PV Society. The training will be delivered online from 11:00 AM to 13:30 PM (CEST) on September 8, 2023. Interested in joining? https://lnkd.in/dt-J53Bf **PVpharm is also organizing in-house training in pharmacovigilance for pharmaceutical - [DIA Pharmacovigilance QMS virtual course (18-21 September 2023)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-18-21-september-2023/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 13:00 AM to 17:30 PM (CEST) on September 18 to 21, 2023. The course will employ a mix of informative sessions, real case studies, and hands-on - [José Alberto Ayala Ortiz selected as one of the top ten CEOs of 2023](https://pvpharm.com/jose-alberto-ayala-ortiz-selected-as-one-of-the-top-ten-ceos-of-2023/) - We are very glad to announce that José Alberto Ayala Ortiz has been selected as one of the top ten CEOs of 2023. Industry Tech Outlook has chosen José, a full article has been issued at the magazine website, it can be found here: https://industry-techoutlook.com/magazine/Top-10-CEOs-Of-2023/ Being the CEO of PVpharm, José is a visionary and - [Meet us in September! at Farmaforum (Madrid) and BIOSPAIN (Barcelona)](https://pvpharm.com/meet-us-in-september-at-farmaforum-madrid-and-biospain-barcelona/) - PVpharm is going to participate in the next events of the pharmaceutical and biotechnology industry in Spain. Farmaforum will be held in Madrid from September 19 to 20, and BIOSPAIN will be held in Barcelona from September 26 to 28. Come visit us and let's talk about pharmacovigilance services, safety in clinical trials, audits, quality - [Development substance data request from EMA – Action required by 01-09-2023](https://pvpharm.com/development-substance-data-request-from-ema-action-required-by-01-09-2023/) - As an owner of development substance data in the Extended EudraVigilance Medicinal Product Dictionary (xEVMPD), the EMA is requesting an action by 1st of September 2023. For the unmapped substance data, the EMA is asking organizations to raise a request for the creation of new approved substance data. This activity requires time, expertise and experience - [IV PV TRAINING: unique pharmacovigilance training experience](https://pvpharm.com/iv-pv-training-unique-pharmacovigilance-training-experience/) - PVpharm led the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. This 3rd edition was hosted on May, 2022. - [Faculty at Signal Management training by DIA June 2023](https://pvpharm.com/faculty-at-signal-management-training-by-dia-june-2023/) - On 12-15 June 2023, José Ortiz provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated data mining techniques. • Design - [PVpharm's offsite meeting 2020 (VIDEO)](https://pvpharm.com/pvpharms-offsite-meeting-2020/) - PVpharm was holding the 2020 Offsite meeting at hotel Envia Golf in Almería. Watch the video here! - [PVpharm's offsite meeting 2021: a memorable event (VIDEO)](https://pvpharm.com/pvpharms-offsite-meeting-2021-a-memorable-event/) - PVpharm has enjoyed several sessions where the team has enjoyed sailing on one of the most wonderful landscapes of Spain, the coast of Almeria. - [José Alberto Ayala Ortiz to participate in the AEFI Symposium 2023](https://pvpharm.com/jose-alberto-ayala-ortiz-to-participate-in-the-aefi-symposium-2023/) - We are happy to announce that José Alberto Ayala Ortiz, PVpharm's CEO will be participating in one session of the 2023 Pharmacovigilance symposium organized by AEFI. During the session, José will be talking about safety in food or food supplements. Please take a look to the program at this link: https://www.aefi2023.com/ - [PVpharm starts a new collaboration with the International AIDS Vaccine Initiative (IAVI)](https://pvpharm.com/pvpharm-starts-a-new-collaboration-with-the-international-aids-vaccine-initiative-iavi/) - We are so excited to announce the new collaboration agreement signed by our company with the International AIDS Vaccine Initiative (IAVI) to provide pharmacovigilance and regulatory consulting. IAVI is a nonprofit scientific research organization that develops vaccines and antibodies for HIV, tuberculosis, emerging infectious diseases (including COVID-19), and other neglected diseases, with a clear commitment to develop affordable and accesible solutions - [Online EVWeb training 22-26 May 2023](https://pvpharm.com/online-evweb-training-22-26-may-2023/) - Isabella Pallagiano from PVpharm will be participating as a trainer, together with Calin Lungu and Vojtech Kvita in the next EVWeb training on 22-26 May 2023. The training will be delivered online in the morning time (9:00-13:30 CEST). The training is targeted to: -Users who have to report and analyse suspected adverse reactions in the - [We are in the press! El Economista](https://pvpharm.com/we-are-in-the-press-el-economista/) - PVpharm is in "El Economista" on 9th May 2023, the news diary published an article about PVpharm; where our CEO, José Alberto Ayala Ortiz, introduces our company, explains what pharmacovigilance is and how does PVpharm deal with different regulations. PVpharm is a global reference in Pharmacovigilance: https://www.eleconomista.es/branded-content/noticias/12258631/05/23/jose-alberto-ayala-ortiz-pvpharm-somos-una-referencia-global-en-el-campo-de-la-farmacovigilancia.html You can follow us on LinkedIn and learn more - [PVpharm initiates a collaboration with the Leiden University Medical Center (LUMC) in the Netherlands](https://pvpharm.com/pvpharm-initiates-a-collaboration-with-the-leiden-university-medical-center-lumc-in-the-netherlands/) - We are happy to announce that PVpharm have enter in a new agreement with Leiden University Medical Center (LUMC) to provide safety and regulatory consulting. LUMC was formed from a collaboration between the Academic Hospital Leiden and the Faculty of Medicine of Leiden University, and provides scientific and material support to first steps of the - [Clinical Trials Information System (CTIS) training 2-5 May 2023](https://pvpharm.com/clinical-trials-information-system-ctis-training-2-5-may-2023/) - The European Commission has informed that the entry into application of the Clinical Trials Regulation (CTR) - [Online XEVMPD training 10-12 May 2023](https://pvpharm.com/online-xevmpd-training-10-12-may-2023/) - José Alberto Ayala Ortiz, Isabella Pallagiano and Monika Gappa from PVpharm will be participating as trainers in the next XEVMPD training on 10-12 May 2023. The training will be delivered online in the afternoon time (14:00-18:00 CEST). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission - [Training Online XEVMPD for SPONSORS 4-5 May 2023](https://pvpharm.com/training-online-xevmpd-for-sponsors-4-5-may-2023/) - This training will focus on explaining the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM) and the use of the XEVMPD data entry tool (EVWEB). - [DIA Pharmacovigilance System Master File (PSMF) and Global PSMF virtual courses (18-20 April 2023)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-and-global-psmf-virtual-courses-18-20-april-2023/) - José Ortiz will be participating as a trainer together with Marcela Fialova in the Pharmacovigilance System Master File (PSMF) and Global PSMF courses organized by DIA. The training will be delivered online from 9:00 AM to 1:00 PM (CEST) on April 18 to 20, 2023. These virtual live training courses covers essential concepts and guidance - [PVpharm participates in “Feria de Empleo 2023” at the University of Almería](https://pvpharm.com/pvpharm-participates-in-feria-de-empleo-2023-at-the-university-of-almeria/) - PVpharm will be participating in the “Feria de Empleo 2023”, along with other companies and organizations from Almería like Cosentino, Cajamar, Kimitec, FAAM or Verdiblanca. This job fair dedicates two days in which local companies have the opportunity to make themselves known in a closer way and thus create a common space where both, the - [PVpharm to provide pharmacovigilance and CTIS support to the Centre for Human Drug Research of the Netherlands (CHDR).](https://pvpharm.com/pvpharm-to-provide-pharmacovigilance-and-ctis-support-to-the-center-for-human-drug-research-of-the-netherlands-chdr/) - We are happy to announce that PVpharm have enter in a new agreement with Centre for Human Drug Research (CHDR) to provide safety and regulatory consulting. This prestigious foundation, based in Leiden (NL) and with three decades of history, provide scientific and material support to first steps of the drug development in humans (phase I - [PVpharm team summer offsite meeting in Almeria 2022](https://pvpharm.com/pvpharm-team-summer-offsite-meeting-in-almeria-2022/) - The PVpharm team had a meeting in Almería on the 29th and 30th of August 2022. The team did several activities, including a hiking route from Arrecife de las Sirenas to Cala Rajá, in the Natural Park of Cabo de Gata. The route was coached by AGata Verde, an innovative project in the field of - [PVpharm participates in the 2022 European Researchers’ Night](https://pvpharm.com/pvpharm-participates-in-the-2022-european-researchers-night/) - The European Researchers' Night is a Europe-wide public event, which displays the diversity of science and its impact on citizens' daily lives in fun, inspiring ways. This year, the event will take place in 25 countries on Friday 30 September 2022. The European Researchers' Night aims to: -bring research and researchers closer to the public-promote - [PVpharm at Farmaforum 2022 (Video)](https://pvpharm.com/pvpharm-at-farmaforum-2022-video/) - PVpharm participated in the 2022 edition of FARMAFORUM. PVpharm presented their services. We created a VIDEO that you can see below. Pharmacovigilance and quality services GVP, GCP, GDP and GMP: As a Pharmacovigilance service provider, PVpharm offers a full range of PV services for the pharmaceutical industry, sponsors of clinical trials and other service provider - [Online XEVMPD training 13-15 and Sponsors XEVMPD 16-17 Feb 2023](https://pvpharm.com/online-xevmpd-training-13-15-and-sponsors-xevmpd-16-17-feb-2023/) - José Ortiz will be participating as a trainer in the next XEVMPD training on 14-16 Feb 2022. The training will focus on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products. - [Faculty at Signal Management training by DIA November 2022](https://pvpharm.com/faculty-at-signal-management-training-by-dia-november-2022/) - On 21-24 November 2022, José Ortiz provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated data mining techniques. • Design - [DIA QPPV forum 2022 - No slides presentation](https://pvpharm.com/dia-qppv-forum-2022-no-slides-presentation/) - José Ortiz, PVpharm CEO, participated one more time as a speaker in the QPPV forum 2022 organized by DIA. https://www.diaglobal.org/en/conference-listing/meetings/2022/11/global-forum-for-qualified-persons-for-pharmacovigilance-qppv José presented in the Session 2: Pharmacovigilance System Oversight on 09 Nov 2022 9:00 AM – 09 Nov 2022 10:30 AM together with other key speakers as: -Sina Schader, DrMed EU and UK QPPV Abbvie, - [The University of Valladolid counts on PVpharm as experts for its PV course](https://pvpharm.com/the-university-of-valladolid-counts-on-pvpharm-as-experts-for-its-pv-course/) - The FUNGE will organize the XXVI Edition of the well-known "Pharmacovigilance for Healthcare Professionals" course. On this occasion, Jose Alberto Ayala Ortiz, CEO of PVpharm, will participate as a trainer. - [Round table and discussion - Differences between Phase III and Phase IV Drug Safety and Pharmacovigilance - University of Valladolid](https://pvpharm.com/round-table-and-discussion-differences-between-phase-iii-and-phase-iv-drug-safety-and-pharmacovigilance-university-of-valladolid/) - José Alberto Ayala Ortiz, PVpharm CEO, will participate together with Andrea Álvarez, QPPV of FAES FARMA in a Round table and discussion about "Differences between Phase III and Phase IV Drug Safety and Pharmacovigilance" organized by the University of Valladolid. The conference will be held on 17th November 2022 at 18:00 CET, and it is - [DIA Pharmacovigilance System Master File (PSMF) virtual course (2-3 November 2022)](https://pvpharm.com/dia-pharmacovigilance-system-master-file-psmf-virtual-course-2-3-november-2022/) - José Ortiz will be participating as a trainer together with Marcela Fialova and Claire Longman, MSc Interim Head of GCP and Senior Pharmacovigilance Inspector at the Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom in the Pharmacovigilance System Master File (PSMF) course organized by DIA. The training will be delivered online from 1:00 PM - [Meet us at Farmaforum 4-5 October 2022!](https://pvpharm.com/meet-us-at-farmaforum-4-5-october-2022/) - PVpharm will participate as an exhibitor in the next edition of Farmaforum, one of the most important events of the Pharmaceutical Industry in Spain. The event will be held in Madrid at IFEMA on the 4th and 5th of October 2022. We are so excited and impatiently anticipating the day of the event. If you decide - [José Ortiz to participate as a speaker in the DIA QPPV forum 2022](https://pvpharm.com/jose-ortiz-to-participate-as-a-speaker-in-the-dia-qppv-forum-2022/) - José Ortiz, PVpharm CEO will participate one more time as a speaker in the next QPPV forum organized by DIA. You can find more information in the link: https://www.diaglobal.org/en/conference-listing/meetings/2022/11/global-forum-for-qualified-persons-for-pharmacovigilance-qppv José will be presenting in the Session 2: Pharmacovigilance System Oversight on 09 Nov 2022 9:00 AM – 09 Nov 2022 10:30 AM https://www.diaglobal.org/en/conference-listing/meetings/2022/11/global-forum-for-qualified-persons-for-pharmacovigilance-qppv/agenda/09/session-2-pharmacovigilance-system-oversight?ref=Session2PharmacovigilanceSystemOversight About the - [DIA Pharmacovigilance QMS virtual course (19-22 September 2022)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-19-22-september-2022/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 9:00 AM to 01:30 PM (CEST) on September 19 to 22, 2022. The course will employ a mix of informative sessions, real case studies, and hands-on - [CTIS for sponsors of clinical trials](https://pvpharm.com/ctis-for-sponsors-of-clinical-trials/) - Sponsors of clinical trials in the EU should be aware that the EMA’s Management Board, on 31 January 2022 established a harmonized approach to submission, assessment, and authorization of clinical trial applications. - [PVpharm to present a key trending subject at Farmaforum 2022](https://pvpharm.com/pvpharm-to-present-a-key-trending-subject-at-farmaforum-2022/) - In the next edition (October 2022), PVpharm will not only participate as an exhibitor but also as a speaker, leading one of the conferences of this benchmark event. - [III PV TRAINING: Leading experts make success possible](https://pvpharm.com/iii-pv-training-leading-experts-make-success-possible/) - PVpharm led the way in pharmacovigilance training by innovatively organizing another edition of its Pharmacovigilance Training. This 3rd edition was hosted on May, 2022. - [PVpharm becomes member of ASEBIO](https://pvpharm.com/pvpharm-becomes-member-of-asebio/) - PVpharm has enjoyed several sessions where the team has enjoyed sailing on one of the most wonderful landscapes of Spain, the coast of Almeria. - [Time to meet in person again: PV TRAINING III EDITION](https://pvpharm.com/pv-training-iii-edition-madrid/) - PVpharm organizes its successful Pharmacovigilance Training. This 3rd edition will be hosted in Madrid on May 30 and 31, 2022, with the option of attending online. - [International Women's Day at PVpharm](https://pvpharm.com/international-womens-day-at-pvpharm/) - PVpharm is made up of women who battle every day to show the world their strength and worth. Today more than ever, we have in mind all those girls and women who still do not have access to opportunities - [Lecturer at the International Pharma Industry Congress - LATAM 2021](https://pvpharm.com/lecturer-at-the-international-pharma-industry-congress-latam-2021/) - José Ortiz will be one of the speakers at the International Pharmaceutical Industry Congress - Latin America 2021. This is the most important event of the Pharmaceutical Industry in the region. - [Online XEVMPD training 14-16 Feb 2022](https://pvpharm.com/online-xevmpd-training-14-16-feb-2022/) - José Ortiz will be participating as a trainer in the next XEVMPD training on 14-16 Feb 2022. The training will focus on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products. - [New training Online XEVMPD for SPONSORS 17 Feb 2022](https://pvpharm.com/new-training-online-xevmpd-for-sponsors-17-feb-2022/) - This training will focus on explaining the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM) and the use of the XEVMPD data entry tool (EVWEB). - [Is the Local Medical Literature Search in Pharmacovigilance really an obligation?](https://pvpharm.com/is-the-local-medical-literature-search-in-pharmacovigilance-really-an-obligation/) - It is well known that the medical literature is a significant source of information for the monitoring of the safety profile and of the risk-benefit balance of medicinal products. However, we may have doubts about whether it is really mandatory or not. And indeed, yes, it is an obligation. The European Medicines Agency confirms this - [DIA Pharmacovigilance QMS virtual course (25-28 January)](https://pvpharm.com/dia-pharmacovigilance-qms-virtual-course-25-28-january/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 9:00 AM to 01:30 PM (CEST) on January 25 to 28, 2022. The course will employ a mix of informative sessions, real case studies, and hands-on - [Christmas 2021: the most unique moments](https://pvpharm.com/christmas-2021-the-most-unique-moments/) - PVpharm has enjoyed several sessions where the team has enjoyed sailing on one of the most wonderful landscapes of Spain, the coast of Almeria. - [CTIS Reminder for Sponsors: Register your organization and Administrator!](https://pvpharm.com/ctis-reminder-for-sponsors-register-your-organization-and-administrator/) - The go-live of CTIS on 31 January 2022 is now less than two months away, and organisations throughout Europe and beyond are undergoing preparations for CTIS. Users are reminded that certain preparatory steps must be taken before it is possible to use CTIS. Sponsor organisations opting for the organisation-centric approach that are not yet registered - [Christmas 2021 arrives at PVpharm](https://pvpharm.com/christmas-2021-arrives-at-pvpharm/) - PVpharm has enjoyed several sessions where the team has enjoyed sailing on one of the most wonderful landscapes of Spain, the coast of Almeria. - [PVpharm invited to ICARO Awards 2021 from University of Almería](https://pvpharm.com/pvpharm-invited-to-icaro-awards-2021-from-university-of-almeria/) - PVpharm has been invited to the ICARO Awards from the University of Almería (UAL) one more year. This act recognises the importance of the alliance between PVpharm and the highest educational institution in Almería, the University. - [PVpharm participates in the 8th Annual Pharmacovigilance Symposium](https://pvpharm.com/pvpharm-participates-in-8th-annual-pharmacovigilance-symposium/) - PVpharm is pleased to inform that José Ortiz, will be a speaker in the online 8th Annual Pharmacovigilance Symposium webinar with the theme “Redefining Pharmacovigilance Frontiers for Augmenting Healthcare”, carried out by Pharmacovigilance Council of the Indian Society for Clinical Research (ISCR). - [New Clinical Trials Information System (CTIS): key areas](https://pvpharm.com/new-clinical-trials-information-system-ctis-key-areas/) - The European Commission has informed that the entry into application of the Clinical Trials Regulation (CTR) and hence the go-live date for the CTIS will be on 31 January 2022. - [PVpharm on the EMA course: Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU](https://pvpharm.com/pvpharm-on-the-ema-course-mandatory-use-of-iso-ich-e2br3-individual-case-safety-reporting-in-the-eu/) - PVpharm is pleased to inform that José Ortíz, will be a trainer in the course "Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU: Practical training course with the EudraVigilance system" carried out by the European Medicines Agency (EMA). - [PVpharm contributes to a recent article about the Covid vaccine](https://pvpharm.com/pvpharm-contributes-to-a-recent-article-about-the-covid-vaccine/) - "Pharmacovigilance in times of COVID-19 vaccines", is an article published in the Spanish journal Pharmatech and in which José Alberto Ayala Ortiz has been co-author. The world is facing the unprecedented challenge of the SARS-CoV-2 pandemic. The hope for a normal life relied on vaccines is compromised by messages that question them. For this reason, - [DIA Pharmacovigilance QMS virtual course (21-24 September)](https://pvpharm.com/pharmacovigilance-qms-virtual-course-21-24-september/) - José Ortiz will be participating as a trainer together with Wendy Huisman in the Pharmacovigilance Quality Management System course organized by DIA. The training will be delivered online from 1:30 PM to 6:00 PM (CEST). The course will employ a mix of informative sessions, real case studies, and hands-on interactive exercises where attendees will be - [Online XEVMPD training 13-15 September 2021](https://pvpharm.com/online-xevmpd-training-13-15-september-2021/) - José Ortiz will be participating as a trainer in the next XEVMPD training on 13-15 September 2021. The training will be delivered online in the morning time (9:00-13:00 CEST). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format - [Risk Management Plan (EU-RMP) Creation Virtual Live Training Course](https://pvpharm.com/risk-management-plan-eu-rmp-creation-virtual-live-training-course/) - Jan Kolouch will be participating as a trainer in the next Risk Management Plan training on 14-16 September 2021 organized by DIA. The training will be delivered online in the morning time (09:00-13:00 CEST). This virtual live course is aimed at the practical aspects of the EU Risk Management Plan (EU-RMP) creation process. We will - [Online XEVMPD training 14-16 June 2021](https://pvpharm.com/online-xevmpd-training-14-16-june-2021/) - José Ortiz will be participating as a trainer in the next XEVMPD training on 14-16 June 2021. The training will be delivered online in the afternoon time (14:00-18:00 CEST). The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format - [José Ortiz to participate in the AEFI Symposium 2021](https://pvpharm.com/jose-ortiz-to-participate-in-the-aefi-symposium-2021/) - We are happy to announce that José Ortiz, PVpharm's CEO will be participating in one session of the 2021 Pharmacovigilance symposium organized by AEFI. During the session, José will be talking about outsourcing of pharmacovigilance activities. Please take a look to the program at this link: https://www.aefi2021.com/ - [Online XEVMPD training 19-21 April 2021](https://pvpharm.com/online-xevmpd-training-19-21-april-2021/) - José Ortiz will be participating as a trainer together with Dr. Calin Lungu in the next XEVMPD training on 19-21 April 2021. The training will be delivered online. The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying the format of - [PVpharm provides support to the UCLouvain for COVID-19 phase II study project](https://pvpharm.com/pvpharm-provides-support-to-the-uclouvain-for-covid-19-phase-ii-study-project/) - We are happy to announce that PVpharm has been selected to provide safety support for a research project coordinated by the Catholic University of Louvain (UCLouvain) for a COVID-19 Phase II study. PVpharm will be supporting the clinical safety function with pharmacovigilance, report submission, safety report writing, Eudravigilance, CTIS and other PV and administrative related - [PVpharm opens an office in Prague](https://pvpharm.com/pvpharm-opens-an-office-in-prague/) - We are happy to announce that PVpharm is opening an office in Prague (Czech Republic). For all our partners and collaborators we are welcoming you at our new location! PVpharm S.L. - Prague, Smichoff, Plzeňská 3350/18, 150 00 Praha 5-Smíchov, Chequia - [PVpharm provides Local Contact Persons for Pharmacovigilance (LCPPVs) in the EU and the UK](https://pvpharm.com/pvpharm-provides-local-contact-persons-for-pharmacovigilance-lcppvs-in-the-eu-and-the-uk/) - PVpharm provides the Local Contact Person for Pharmacovigilance (LCPPV) in all EU countries and UK, besides we can also provide the EU Qualified Person for Pharmacovigilance (EU QPPV), UK QPPV and and Deputy persons with large knowledge and experience of the industry. Any medicinal product cannot be authorized in the EU without a Qualified Person - [Open positions: Senior Pharmacovigilance officer](https://pvpharm.com/open-positions-senior-pharmacovigilance-officer/) - PVpharm is searching for a Senior Pharmacovigilance officer to provide support for clients and work closely within PVpharm's team in our headquarters in Almería. This position requires documented experience in Pharmacovigilance, organizational and team management skills and willingness to drive the team and the organization to the highest level. Job descriptionAs a senior pharmacovigilance officer you will - [PVpharm selected as one of the top ten companies providing compliance services and transforming business](https://pvpharm.com/pvpharm-selected-as-one-of-the-top-ten-companies-providing-compliance-services-and-transforming-business/) - We are very glad to announce that PVpharm has been selected as one of the top ten companies providing compliance services and transforming business. The European edition of PharmaTech Outlook www.pharmatechoutlook.com has choosen us, a full article has been issued at the magazine website, it can be found here: https://compliance-europe.pharmatechoutlook.com/vendor/pvpharm-solving-the-riddle-of-pharmacovigilance-compliance--cid-1039-mid-107.html This recognition is coming in - [QMS virtual course - 26-29 January 09.00-13.30 CEST](https://pvpharm.com/qms-virtual-course-26-29-january-09-00-13-30-cest/) - José Ortiz will be participating together with Brian Edwards in the faculty of the QMS training course organized by DIA. At the conclusion of this virtual live course, participants will be able to: • Describe how to design, develop, and manage a Quality System related to Pharmacovigilance System • Explain the components of the Pharmacovigilance - [Entrevista a José Alberto Ayala Ortiz - Visitadores Médicos Digitales (Spanish Video)](https://pvpharm.com/entrevista-a-jose-alberto-ayala-ortiz-visitadores-medicos-digitales-spanish-video/) - Today we share this interview in Spanish, where José Alberto Ayala Ortiz is invited in an interview on "Visitadores Médicos Digitales" by Miguel Ángel Martínez Barreira. Please watch the video here. PVpharm is also organizing in-house trainings in pharmacovigilance for pharmaceutical companies and CROs, please contact us for further information. - [Jose Ortiz at the European Pharmacovigilance Congress 2020](https://pvpharm.com/jose-ortiz-at-the-european-pharmacovigilance-congress-2020/) - We are delighted to announce that José Alberto Ayala Ortiz, PVpharm's CEO, will be participating in the European Pharmacovigilance Congress 2020 organized by the Pharma Education Center. You can find the link to the Congress here: https://www.pharmaeducationcenter.it/wp-content/uploads/2020/11/EUPV_Final_2020-1.pdf José will be participating in two round tables on the 27th of November:-Eudravigilance EVDAS updates-Local VS Global PV - [PVpharm invited to ICARO Awards from University of Almería](https://pvpharm.com/pvpharm-invited-to-icaro-awards-from-university-of-almeria/) - We are very happy to announce that PVpharm has been invited to the ICARO Awards from the University of Almería (UAL). This act recognises the importance of the alliance between PVpharm and the highest educational institution in Almería, the University. Just only during the year 2020, PVpharm has hosted three trainee positions, one of them - [PVpharm joining ISoP](https://pvpharm.com/pvpharm-joining-isop/) - José Ortiz CEO of PVpharm has become member of the International Society of Pharmacovigilance (ISoP). The International Society of Pharmacovigilance (ISoP) is a professional, independent, non-profit society, open to anyone with an interest in the safe and effective use of medicinal products. The nature of the global pharmacovigilance landscape and societal context has been rapidly - [Online XEVMPD training 23-25 November 2020](https://pvpharm.com/online-xevmpd-training-23-25-november-2020/) - José Ortiz will be participating as a trainer together with Raj K. Bains and Calin Lungu in the next XEVMPD training on 23-25 November 2020. The training will be delivered online. The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying - [Online XEVMPD training 21-23 October 2020](https://pvpharm.com/online-xevmpd-training-21-23-october-2020/) - José Ortiz will be participating as a trainer together with Raj K. Bains and Calin Lungu in the next XEVMPD training on 21-23 October 2020. The training will be delivered online. The training focuses on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, applying - [José Ortiz to participate as a speaker in the DIA QPPV forum 2020](https://pvpharm.com/jose-ortiz-to-participate-as-a-speaker-in-the-dia-qppv-forum-2020/) - José Ortiz, PVpharm CEO will participate as a speaker in the next QPPV forum organized by DIA. You can find more information in the link: https://www.diaglobal.org/en/conference-listing/meetings/2020/10/global-forum-for-qualified-persons-for-pharmacovigilance-qppv About the QPPV forum: In a changing and expanding world, this is still the only forum designed for QPPVs by QPPVs, now in its 14th year and still going - [PVpharm joins FAEEM](https://pvpharm.com/pvpharm-joins-faeem/) - PVpharm recently joined FAEEM (Almeria Foundation for Business Excellence). On 18th September 2020, José Alberto Ayala Ortiz and Elena Marín Cassinello participated in the governing board meeting that formally accepted PVpharm into FAEEM structure. FAEEM was created in 2007 by the Commission for Business Excellence of the Chamber of Commerce of Almería. The Foundation chaired - [QMS virtual course in September - NEW DATES - 22-25 September 09.00-13.00 CEST](https://pvpharm.com/qms-virtual-course-in-september-new-dates-22-25-september-09-00-13-00-cest/) - José Ortiz will be participating together with Brian Edwards in the faculty of the QMS training course organized by DIA. At the conclusion of this virtual live course, participants will be able to: • Describe how to design, develop, and manage a Quality System related to Pharmacovigilance System • Explain the components of the Pharmacovigilance - [Faculty at Signal Management training by DIA](https://pvpharm.com/faculty-at-signal-management-training-by-dia/) - On 7-10 September 2020, José Ortiz, and Jan Kolouch from PVpharm provided the training faculty for the Signal Management training organized by DIA. This training provides knowledge over Signal Management to the participants, so they can apply the basic concepts and principles of signal detection in pharmacovigilance, from simple visualisation and tabulation methods to sophisticated - [PVpharm's team returning to the Office: Lessons learned from remote working under COVID-19 restrictions](https://pvpharm.com/pvpharms-team-returning-to-the-office-lessons-learned-from-remote-working-under-covid-19-restrictions/) - After a period of working from home because of the COVID-19 situation, we are happy to announce the re-incorporation of the PVpharm's team members to the Almería office (HQ). The team will be back in the office by Monday 22nd June, after a period of full remote working initiated in April following the instructions of - [Pharmacovigilance Audits](https://pvpharm.com/pharmacovigilance-audits/) - EU Guidelines on Good Pharmacovigilance Practices (GVP Module IV), mandate that all Marketing Authorisation Holders (MAHs) perform audits of their Pharmacovigilance Systems. PVpharm provides a risk-based Pharmacovigilance Audit Service, which focuses on the areas of highest risk to an organisation’s pharmacovigilance system, taking into account applicable local regulatory requirements. Our approach is risk and process based, our objective - [EVWEB training in Amsterdam December 2018](https://pvpharm.com/evweb-training-in-amsterdam-december-2018/) - Amsterdam is the next place where the DIA is organizing an EVWeb training. The course will take place at the BCN Amsterdam Arena on December 10th to 12th. José Alberto Ayala Ortiz is participating as trainer for this course. The EVWeb hands-on training "The new EudraVigilance system and the electronic reporting of ICSRs in the ISO/ICH E2B(R3) format: hands-on training course, Amsterdam, The Netherlands" - [EVWEB and XEVMPD training in London November 2018](https://pvpharm.com/evweb-and-xevmpd-training-in-london-november-2018/) - The DIA is organizing an EVWeb and XEVMPD training course at EMA in London in June, respectively on the dates 12-14 and 15-16. José Alberto Ayala Ortiz is participating as trainer for these courses. The EVWeb hands-on training "The NEW EudraVigilance System and the electronic reporting of ICSRs in the ISO/ICH E2B(R3) format" covers the functionalities of the new EudraVigilance web application (EVWEB). It - [PVpharm to participate at EUPV Congress in Milano](https://pvpharm.com/pvpharm-to-participate-at-eupv-congress-in-milano/) - PEC – Pharma Education Center S.r.l. warmly invites PV professionals from all over the world to the “European Pharmacovigilance Congress – 2nd Edition” which will be held on November 29-30, 2018in Milan, Italy. The core of the 2nd European Pharmacovigilance congress are the significant changes and challenges due to the EUDRAVIGILANCE implementation. PVpharm will be participating in the Congress. José Ortiz, our experienced trainer, will present a - [Audit on Signal Detection at Perrigo](https://pvpharm.com/audit-on-signal-detection-at-perrigo/) - José Alberto Ayala Ortiz has been performing an audit dedicated exclusively on the Signal Detectionprocess at Perrigo. The audit was held at their main offices. The Signal Detection process was reviewed during the two days, and opportunities for improvement were proposed to the team. The main objective was to to contribute to improving risk management, control, and governance processes. PVpharm - [Pharmacovigilance training 1st edition review.](https://pvpharm.com/pharmacovigilance-training-1st-edition-review/) - PVpharm organized a Pharmacovigilance training course on October 18th and 19th 2018. We had the honour to have as trainers: Mariano Madurga (a well known professional with more than 30 years of dedicated experience in pharmacovigilance, being an official of the Ministry of health/AEMPS and developing the pharmacovigilance Network in Spain), Calin Lungu (Dr. Lungu has worked more than 20 years in - [Signal detection training at CHEMO](https://pvpharm.com/signal-detection-training-at-chemo/) - Signal detection training at CHEMO October 26, 2018 |PVpharm José Alberto Ayala Ortiz has been training the CHEMO Signal Detection team in Signal Detection. The training was held earlier this week at CHEMO offices in Madrid. This was a one day training held in-house, the objective of the training/workshop was to focus on Chemo’s Eudravigilance profile, EVDAS and Signal Management - [EVWEB training in Amsterdam February 2019](https://pvpharm.com/evweb-training-in-amsterdam-february-2019/) - The DIA is organizing an EVWEB training in which José Alberto Ayala Ortiz will participate as a trainer. The course will be taking place in Amsterdam, exactly at the BCN Amsterdam Arena from the 11th to the 13th February 2019.​SMLXL The hands-on training “The NEW EudraVigilance System and the electronic reporting of ICSRs in the - [Meet us at Farmaforum!](https://pvpharm.com/meet-us-at-farmaforum/) - PVpharm will participate as an exhibitor in the 6th edition of Farmaforum, one of the most important events of the Pharmaceutical Industry in Spain. The event will be held in Madrid at IFEMA (Pabellón 8-Feria de Madrid) on the 28th and 29th of March. We are so excited and impatiently anticipating the day of the event. - [PVpharm provides Qualified Person for Pharmacovigilance Services (EU QPPV)](https://pvpharm.com/pvpharm-provides-qualified-person-for-pharmacovigilance-services-eu-qppv/) - PVpharm provides EU Qualified Person for Pharmacovigilance (EU QPPV) and Deputy EU QPPV with large knowledge and experience of the industry. Besides, PVpharm has contact persons for pharmacovigilance in several EU countries Any medicinal product cannot be authorized in the EU without a Qualified Person for Pharmacovigilance (EU QPPV). The EU QPPV is responsible for - [We are in the press!](https://pvpharm.com/we-are-in-the-press/) - Last Sunday, 10th March 2019, the news diary “La Razón” published an article about PVpharm; where our CEO, José Alberto Ayala Ortiz, introduces our company, explains what pharmacovigilance is and how does PVpharm deal with different regulations. You can follow us on Linkedin and learn more about us clicking here. - [PV Training II Edition is here!](https://pvpharm.com/pv-training-ii-edition-is-here/) - After the success of the first edition of the I Pharmacovigilance Training, PVpharm is organizing its Pharmacovigilance Training II Edition on the 9th and 10th of May 2019 in Madrid.The course will cover different trending topics in PV; focusing on Audits, Inspections, the QPPV role and Eudravigilance and Signal Detection. We will also cover the new - [EVWEB Prague 15th-17th May](https://pvpharm.com/evweb-prague-15th-17th-may/) - José Alberto Ayala Ortiz, the CEO of PVpharm, will be participating as an instructor in the EVWEB training organized by the DIA association in Prague from the 15th till the 17th May. This training, "The NEW EudraVigilance System and the electronic reporting of ICSRs in the ISO/ICH E2B (R3) format", will involve the functionalities of - [PVpharm Pharmacovigilance Training II edition review](https://pvpharm.com/pvpharm-pharmacovigilance-training-ii-edition-review/) - On 9th and 10th May 2019, PVpharm provided a pharmacovigilance training in Madrid. We had the honour to have as trainers: Mariano Madruga: a well known professional with more than 30 years dedicated experience in pharmacovigilance, being an official of the Ministry of health/AEMPS and developing the pharmacovigilance Network in Spain.Calin Lungu: Dr. Lungu has - [EVWeb and XEVMPD Madrid (20th-24th May)](https://pvpharm.com/evweb-xevmpd-madrid-20th-24th-may/) - Our CEO, José Alberto Ayala Ortiz participated as an intructor in the EVWEB and XEVMPD training. The course was offered by The European Medicines Agency (EMA) and took place in Madrid from 20th to 24th May. The EVWEB hands-on training course "The new EudraVigilance system and the electronic reporting of individual case safety reports in - [EVWEB and XEVMPD Basel (24th - 28th June)](https://pvpharm.com/evweb-and-xevmpd-basel-24th-28th-june/) - From the 24th to the 26th June, the European Medicines Agency (EMA) provided an EVWEB training course in Basel, Switzerland. PVpharm's CEO, José Alberto Ayala Ortiz had the honor to participate as one of the instructors. The training focused mainly on explaining the guidance and specifically the mandatory data elements necessary for the electronic submission - [EVWEB and XEVMPD Training in Amsterdam (16th-20th September)](https://pvpharm.com/evweb-and-xevmpd-training-in-amsterdam-16th-20th-september/) - From the 16th to the 20th September, José Alberto Ayala Ortiz will be participating as an instructor on the EVWEB and XEVMPD training courses provided by the European Medicines Agency (EMA) in Amsterdam. From the 16th to the 18th September, a hands-on Training Course using the EudraVigilance System will be provided. This training course covers:-Explanation - [Signal Management in Pharmacovigilance 18-19 November Berlin](https://pvpharm.com/signal-management-in-pharmacovigilance-18-19-november-berlin/) - PVpharm is happy to inform that José Alberto Ayala Ortiz will be training a DIA course in Signal Management 18-19 November in Berlin. Looking for PV learning opportunities still in 2019? Join this Intermediate Course for professionals with 2-3 years of experience in PV or related functions and learn: The concepts of signal detection and signal management and how to apply - [PVpharm in PIPA conference 2019](https://pvpharm.com/pvpharm-in-pipa-conference-2019/) - On Wednesday 2nd - Thursday 3rd October 2019 PVpharm participated at the PIPA conference in Stratford Manor, near Birmingham. Jose Alberto Ayala Ortiz, PVpharm CEO, was talking about Signal Detection using EVDAS. PVpharm also provides in-house trainings for pharmaceutical companies and CROs. For further information, please contact us. - [ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU: Hands-on Training Course using the EudraVigilance System Madrid (25th-27th March)](https://pvpharm.com/iso-ich-e2br3-individual-case-safety-reporting-in-the-eu-hands-on-training-course-using-the-eudravigilance-system-madrid-25th-27th-march/) - PVpharm is pleased to inform that our CEO, Jose Alberto Ayala Ortiz, will be participating as an instructor in a hands-on training course on the ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU. The course will take place in Madrid from 25th to 27th of March and will provide the extensive information regarding EMA - [PVpharm participates in Nordic PV Day](https://pvpharm.com/pvpharm-participates-in-nordic-pv-day/) - On Thursday 24th October 2019 PVpharm participated at the Nordic Pharmacovigilance Day conference in Copenhagen, Denmark. Jose Alberto Ayala Ortiz, PVpharm CEO, was talking about Signal Detection using EVDAS. It was very nice to meet with former colleagues from the Danish Medicines Agency! PVpharm also provides in-house trainings for pharmaceutical companies and CROs. For further - [PVpharm opens an office in Madrid](https://pvpharm.com/pvpharm-opens-an-office-in-madrid/) - We are happy to announce that PVpharm is opening an office in Madrid. For all our partners and collaborators we are welcoming you at our new location! PVpharm S.L. Núñez de Balboa, 35 Esquina Goya 5º Oficina A4 – 28001 Madrid - [Merry Christmas and a Prosperous New Year!](https://pvpharm.com/merry-christmas-and-a-prosperous-new-year/) - Dear all, on behalf of the PVpharm Team I would like to wish you a Merry Christmas and a Prosperous New Year! - [COVID-19: Business continuity actions at PVpharm](https://pvpharm.com/covid-19-business-continuity-actions-at-pvpharm/) - Let's help everyone stop COVID-19! At PVpharm we adopted business continuity actions in order to save the health of the people working in PVpharm and provide continuation of our PV services to our dear customers. PVpharm is following the recommendations of the Spanish Health Authority, that is recommending to restrict movement of people due to - [PHARMACOVIGILANCE TRAINING III Edition - Madrid 21-22 May 2020, Save the date! - UPDATE: postponed](https://pvpharm.com/pharmacovigilance-training-iii-edition-madrid-21-22-may-2020-save-the-date/) - PVpharm is organizing the III Edition of the PHARMACOVIGILANCE TRAINING, this year it will be held in Madrid. The training was originally scheduled for the 21-22 of May 2020, but it has been posponed due to COVID-19. We will publish the new dates very soon. The previous editions in 2018 and 2019 were really successful, - [Remote working instructions at PVpharm](https://pvpharm.com/remote-working-instructions-at-pvpharm/) - COVID-19:REMOTE WORKING INSTRUCTIONS AT PVPHARM Due to the Coronavirus outbreak, PVpharm decided that all employees should work from home. Only under special circumstances it would be allowed to come to the physical offices. We would like to share with the community our rules, our tips, so everyone can benefit of this learning. Please, stay safe ## Pages - [Home](https://pvpharm.com/) - Pharmacovigilance, Clinical safety, Regulatory and Quality solutions for the pharmaceutical industry. PVpharm provide services to Marketing Authorisation Holders, Sponsors of Clinical Trials and other Life science service providers. Our objective is to help the Pharmaceutical industry to comply with Pharmacovigilance, Clinical safety, Regulatory and Quality requirements. We provide global, professional, quick, and flexible solutions to complex, - [Marketing Authorisation Applications (MAA)](https://pvpharm.com/regulatory-affairs/marketing-authorisation-applications-maa/) - Marketing Authorisation Applications (MAA) Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle - [Regulatory Affairs](https://pvpharm.com/regulatory-affairs/) - Regulatory Affairs Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation PVpharm provides comprehensive Regulatory Affairs support to help companies in the health and life sciences sector navigate complex regulatory environments. - [Scientific Advice and Agency interactions](https://pvpharm.com/regulatory-affairs/scientific-advice-and-agency-interactions/) - Scientific Advice and Agency interactions Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life - [Dedicated RA resources](https://pvpharm.com/regulatory-affairs/dedicated-ra-resources/) - Dedicated RA resources Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management - [ Regulatory training](https://pvpharm.com/regulatory-affairs/regulatory-training/) - Regulatory training Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) - [Launch and market notifications](https://pvpharm.com/regulatory-affairs/launch-and-market-notifications/) - Launch and market notifications Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle - [Promotional and non-promotional materials](https://pvpharm.com/regulatory-affairs/promotional-and-non-promotional-materials/) - Promotional and non-promotional materials Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle - [Regulatory database management](https://pvpharm.com/regulatory-affairs/regulatory-database-management/) - Regulatory database management Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management - [Life cycle management (post-authorisation)](https://pvpharm.com/regulatory-affairs/life-cycle-management-post-authorisation/) - Life cycle management (post-authorisation) Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle - [Gap analysis](https://pvpharm.com/regulatory-affairs/gap-analysis/) - Gap analysis Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) - [Dossier preparation and submission](https://pvpharm.com/regulatory-affairs/dossier-preparation-and-submission/) - Dossier preparation and submission Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle - [Regulatory strategy and planning](https://pvpharm.com/regulatory-affairs/regulatory-strategy-and-planning/) - Regulatory strategy and planning Regulatory Affairs Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory database management Promotional and non-promotional materials Launch and market notifications Regulatory training Dedicated RA resources Scientific Advice and Agency interactions Regulatory strategy and planning Dossier preparation and submission Marketing Authorisation Applications (MAA) Gap analysis Life cycle management (post-authorisation) Regulatory - [Artificial Intelligence (AI) & Digital Transformation](https://pvpharm.com/artificial-intelligence-ai-digital-transformation/) - Artificial Intelligence (AI) & Digital Transformation Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Implementation of AI-enabled solutions for Pharmacovigilance, Regulatory and Quality operations PVpharm supports Marketing Authorisation Holders, Sponsors - [PHARMACOVIGILANCE TRAINING VII Edition - Barcelona 2026](https://pvpharm.com/pharmacovigilance-training-vii-edition-barcelona-2026/) - PHARMACOVIGILANCE TRAINING VII Edition Barcelona & Online 12-13 May 2026 Days Hours Minutes The training was held on 12-13 May 2026, see the video here: Video of the 2026 edition Best in class pharmacovigilance event This training is targeted to Pharmacovigilance professionals. The objective is to provide professional knowledge in this area. This year, participants will also - [About us](https://pvpharm.com/about-us/) - About us We are a team of consultants that works independently or collaborate with organizations and consultancies to deliver professional solutions to complex, specialized needs.We are in continuous development and are open for new challenges and collaborations.We stay focusedWe have an innovative and can-do attitudeWe solve the problem with excellence Management team José Alberto Ayala OrtizCEO - [AulaFV](https://pvpharm.com/aulafv/) - El curso se desarrollará en modalidad online durante las tardes de lunes a viernes entre el 16 de marzo al 29 de mayo de 2026. La formación cuenta con un crédito docente de 6 ECTS, con 60 horas de clases presenciales y 90 horas de estudio independiente, garantizando una formación integral con el aval de - [Critical review and summarization of scientific publications](https://pvpharm.com/medical-services/critical-review-and-summarization-of-scientific-publications/) - Critical review and summarization of scientific publications Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients - [Medical Services](https://pvpharm.com/medical-services/) - Medical Services Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation At PVpharm, our Medical Services provide specialised scientific and clinical expertise to support pharmacovigilance, clinical safety and regulatory activities. Our - [Strategic Medical Advice](https://pvpharm.com/medical-services/strategic-medical-advice/) - Strategic Medical Advice Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call Centre service Development - [Development of medical content for educational activities](https://pvpharm.com/medical-services/development-of-medical-content-for-educational-activities/) - Development of medical content for educational activities Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients - [Call Centre service](https://pvpharm.com/medical-services/call-centre-service/) - Call Centre service Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call Centre service Development - [Management of medical inquiries from healthcare professionals and patients](https://pvpharm.com/medical-services/management-of-medical-inquiries-from-healthcare-professionals-and-patients/) - Management of medical inquiries from healthcare professionals and patients Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals - [Systematic bibliographic searches in biomedical databases](https://pvpharm.com/medical-services/systematic-bibliographic-searches-in-biomedical-databases/) - Systematic bibliographic searches in biomedical databases Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call - [Medical review of promotional and non-promotional materials](https://pvpharm.com/medical-services/medical-review-of-promotional-and-non-promotional-materials/) - Medical review of promotional and non-promotional materials Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients - [Preparation and maintenance of standard responses (FAQs)](https://pvpharm.com/medical-services/preparation-and-maintenance-of-standard-responses-faqs/) - Preparation and maintenance of standard responses (FAQs) Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients - [Scientific & Medical Writing](https://pvpharm.com/medical-services/scientific-medical-writing/) - Scientific & Medical Writing Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call Centre service - [Scientific literature search and critical evaluation](https://pvpharm.com/medical-services/scientific-literature-search-and-critical-evaluation/) - Scientific literature search and critical evaluation Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call - [Medical Information Management](https://pvpharm.com/medical-services/medical-information-management/) - Medical Information Management Services Medical Information Management Scientific literature search and critical evaluation Scientific & Medical Writing Preparation and maintenance of standard responses (FAQs) Medical review of promotional and non-promotional materials Critical review and summarization of scientific publications Systematic bibliographic searches in biomedical databases Management of medical inquiries from healthcare professionals and patients Call Centre service Development of medical - [Training](https://pvpharm.com/training/) - Pharmacovigilance training Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation We provide specialized training programs designed to strengthen the competencies of teams involved in pharmacovigilance, clinical safety, and regulatory activities. - [Quality Management](https://pvpharm.com/quality/) - Quality Management Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation PVpharm supports organisations in building and maintaining robust quality systems aligned with international GxP standards. Our Quality Management services help - [Audit Services](https://pvpharm.com/audit-services/) - Audit Services Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation PVpharm offers independent and comprehensive audit services to assess the quality and compliance of pharmacovigilance and clinical safety systems. Our - [Medical Monitoring and Evaluation](https://pvpharm.com/clinical-safety/medical-monitoring-and-evaluation/) - Medical Monitoring and Evaluation Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality and Compliance in Clinical - [Clinical Safety](https://pvpharm.com/clinical-safety/) - Clinical Safety Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation PVpharm supports sponsors, CROs, and biotech companies throughout the clinical development process, ensuring participant protection and regulatory compliance. Our Clinical - [Quality and Compliance in Clinical Safety](https://pvpharm.com/clinical-safety/quality-and-compliance-in-clinical-safety/) - Quality and Compliance in Clinical Safety Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) - [Support for Marketing Authorisation Applications (MMA)](https://pvpharm.com/clinical-safety/support-for-marketing-authorisation-applications-maa/) - Support for Marketing Authorisation Applications (MMA) Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) - [Clinical Safety Training](https://pvpharm.com/clinical-safety/clinical-safety-training/) - Clinical Safety Training Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality and Compliance in - [Sponsor Profile Registration in EudraVigilance](https://pvpharm.com/clinical-safety/sponsor-profile-registration-in-eudravigilance/) - Sponsor Profile Registration in EudraVigilance Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality and - [Legal Representation in the EU / Responsible Person in EudraVigilance](https://pvpharm.com/clinical-safety/legal-representation-in-the-eu-responsible-person-in-eudravigilance/) - Legal Representation in the EU / Responsible Person in EudraVigilance Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing - [CTIS Portal Management](https://pvpharm.com/clinical-safety/ctis-portal-management/) - CTIS Portal Management Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality and Compliance - [Protocol Review and Safety Input](https://pvpharm.com/clinical-safety/protocol-review-and-safety-input/) - Protocol Review and Safety Input Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality - [Safety Management Plan (SMP) and Investigator Brochure (IB)](https://pvpharm.com/clinical-safety/safety-management-plan-smp-and-investigator-brochure-ib/) - Safety Management Plan (SMP) and Investigator Brochure (IB) Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation - [Development Safety Update Reports (DSUR)](https://pvpharm.com/clinical-safety/development-safety-update-reports-dsur/) - Development Safety Update Reports (DSUR) Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality - [SAE and SUSAR Management](https://pvpharm.com/clinical-safety/sae-and-susar-management/) - SAE and SUSAR Management Clinical Safety SAE and SUSAR Management Medical Monitoring and Evaluation Development Safety Update Reports (DSUR) Safety Management Plan (SMP) and Investigator Brochure (IB) Protocol Review and Safety Input CTIS Portal Management Legal Representation in the EU / Responsible Person in EudraVigilance Sponsor Profile Registration in EudraVigilance Clinical Safety Training Support for Marketing Authorisation Applications (MMA) Quality and - [EU and Local QPPV Services ](https://pvpharm.com/pharmacovigilance/eu-and-local-qppv-services-2/) - EU and Local QPPV Services Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR - [Pharmacovigilance](https://pvpharm.com/pharmacovigilance/) - Pharmacovigilance Services Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Pharmacovigilance Clinical Safety Medical Services Regulatory Affairs Audit Services Quality Management Training AI & Digital Transformation Our Pharmacovigilance services ensure continuous monitoring of the safety of medicinal products, from early development through post-marketing. We support Marketing Authorisation - [Quality Management and SOP Development](https://pvpharm.com/pharmacovigilance/quality-management-and-sop-development/) - Quality Management and SOP Development Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR Management - [XEVMPD and IDMP Compliance](https://pvpharm.com/pharmacovigilance/xevmpd-and-idmp-compliance/) - XEVMPD and IDMP Compliance Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR Management - [Post-Authorization Safety Studies (PASS)](https://pvpharm.com/pharmacovigilance/post-authorization-safety-studies-pass/) - Post-Authorization Safety Studies (PASS) Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR - [Medical Literature Monitoring (global and local)](https://pvpharm.com/pharmacovigilance/medical-literature-monitoring-global-and-local/) - Medical Literature Monitoring (global and local) Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local - [SDEA Management and Regulatory Consultancy](https://pvpharm.com/pharmacovigilance/sdea-management-and-regulatory-consultancy/) - SDEA Management and Regulatory Consultancy Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR Management - [Safety Database Management](https://pvpharm.com/pharmacovigilance/safety-database-management/) - Safety Database Management Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR Management & Medical Review - [Pharmacovigilance System Master File (PSMF)](https://pvpharm.com/pharmacovigilance/pharmacovigilance-system-master-file-psmf/) - Pharmacovigilance System Master File (PSMF) Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services - [PSUR, RMP and other Safety Reports](https://pvpharm.com/pharmacovigilance/psur-rmp-and-other-safety-reports/) - PSUR, RMP and other Safety Reports Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local - [Signal Detection and Management (including EVDAS)](https://pvpharm.com/pharmacovigilance/signal-detection-and-management-including-evdas/) - Signal Detection and Management (including EVDAS) Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local - [ICSR Management & Medical Review](https://pvpharm.com/pharmacovigilance/eu-and-local-qppv-services/) - ICSR Management & Medical Review Pharmacovigilance EU and Local QPPV Services ICSR Management & Medical Review Signal Detection and Management (including EVDAS) PSUR, RMP and other Safety Reports Pharmacovigilance System Master File (PSMF) Safety Database Management SDEA Management and Regulatory Consultancy Medical Literature Monitoring (global and local) Post-Authorization Safety Studies (PASS) XEVMPD and IDMP Compliance Quality Management and SOP Development EU and Local QPPV Services ICSR - [Contact](https://pvpharm.com/contact/) - Contact us info@pvpharm.com Linkedin-in Facebook-f Contact form PVpharm offices OFFICES IN SPAIN ALMERÍAPaseo de Almería 81, 1-D04001 AlmeríaSpain MADRIDCalle Princesa, Nº3, Duplicado, Planta 8, Puerta 80828008, MadridSpain OFFICE IN CZECH REPUBLIC PRAGUE Plzeňská 3350/18, 150 00Praha 5-SmíchovCzech Republic OFFICE IN PORTUGALLISBONRua Mouzinho de Silveira, 32, 1250 167LisboaPortugal Newsletter form - [PHARMACOVIGILANCE TRAINING VI Edition - Barcelona 2025](https://pvpharm.com/pharmacovigilance-training-vi-edition-barcelona-2025/) - PHARMACOVIGILANCE TRAINING VI Edition Barcelona & Online 12-13 May 2025 Pharmacovigilance Training VI Edition, Barcelona and Online 12-13 May 2025The event is already finalized, please see the video below This training is targeted to Pharmacovigilance professionals. The objective is to provide professional knowledge in this area. This year, participants will also have the opportunity to send their - [Quality Policy](https://pvpharm.com/quality-policy/) - QUALITY POLICY PVpharm’s CEO is committed to keeping the highest Quality standards in accordance with the directions set out in this policy. The purpose of this policy is to: – Guarantee and Improve the Quality of the services provided, promoting continuous improvement of our services and the management of the company. – Meet and exceed - [Home - Copy](https://pvpharm.com/home-copy/) - Pharmacovigilance, Clinical Safety, Regulatory and Quality Solutions for the pharmaceutical industry PVpharm provide services to Marketing Authorisation Holders, Sponsors of Clinical Trials and other Life science service providers.Our objective is to help the Pharmaceutical industry to comply with Pharmacovigilance, Clinical safety, Regulatory and Quality requirements. We provide global, professional, quick, and flexible solutions to complex, specialized needs. OUR - [Borrador: Home](https://pvpharm.com/borrador-home/) - Pharmacovigilance and regulatory solutions for the pharmaceutical industry PVpharm is a pharmacovigilance service provider based in Spain (EU). We provide services to Marketing Authorisation Holders, Sponsors and to other pharmacovigilance service providers with the objective of helping the Pharmaceutical industry to comply with Pharmacovigilance regulatory requirements. We provide global, professional, quick, and flexible solutions to complex, specialized needs. - [Careers](https://pvpharm.com/careers/) - Jobs and Careers Our Mission is to deliver top-quality services, within the stipulated deadlines, with excellent understanding of the regulatory framework. Our Vision is to become a preferred partner by helping the pharmaceutical industry to comply with Pharmacovigilance, Clinical safety, Regulatory and Quality requirements. We are a young and fast growing organization, with multiple career development opportunities. - [About us - Borrador](https://pvpharm.com/duplicado-about-us-70/) - About us We are a team of consultants that works independently or collaborate with organizations and consultancies to deliver professional solutions to complex, specialized needs.We are in continuous development and are open for new challenges and collaborations.We stay focusedWe have an innovative and can-do attitudeWe solve the problem with excellence With headquarters in Spain, Portugal and - [PHARMACOVIGILANCE TRAINING V Edition - Madrid 2024](https://pvpharm.com/pharmacovigilance-training-v-edition/) - PHARMACOVIGILANCE TRAINING V Edition Madrid & Online 27-28 May 2024 Pharmacovigilance Training V Edition, Madrid and Online 27-28 May 2024 Thank you for your participation! PVpharm organized a hybrid face-to-face/remote training in Madrid on 27-28 May 2024. Don’t miss the Next Edition! More information here very soon! This training is targeted to Pharmacovigilance professionals. The objective is - [Privacy Policy](https://pvpharm.com/privacy-policy/) - PRIVACY POLICY (1st LAYER) DATA PROCESSOR PVPHARM S.L PURPOSE – carry out the necessary commercial and administrative procedures with web Users – send commercial advertisement communications by email, fax, SMS, MMS, social communities, or any other electronic or physical means (if the User has previously given consent), – respond to inquiries and/or provide information requested - [Curso de Introducción a la Farmacovigilancia 1 edición (Compra)](https://pvpharm.com/curso-de-introduccion-a-la-farmacovigilancia-1-edicion-compra/) - [asp_product id="7364"] - [Checkout-Result](https://pvpharm.com/stripe-checkout-result/) - [accept_stripe_payment_checkout] Thank you! Thank you for your purchase! - [Products](https://pvpharm.com/products/) - [asp_show_all_products] - [PHARMACOVIGILANCE TRAINING V EDITION - Madrid 2024 (Landing page)](https://pvpharm.com/pharmacovigilance-training-v-edition-madrid-2024/) - [footer](https://pvpharm.com/footer/) - [PHARMACOVIGILANCE TRAINING IV Edition](https://pvpharm.com/pharmacovigilance-training-iv-edition/) - PHARMACOVIGILANCE TRAINING IV Edition Madrid & Online 19-20 June 2023 The Pharmacovigilance Training IV Edition finalized on 20th June 2023, please contact us for more information about training courses After the successful previous editions, PVpharm is organizing a hybrid face-to-face/remote training in Madrid on 19-20 June 2023. Don’t miss the IV Edition! This training is targeted - [PHARMACOVIGILANCE TRAINING II Edition](https://pvpharm.com/pharmacovigilance-training-ii-edition/) - PHARMACOVIGILANCE TRAINING II Edition Madrid 9-10 May 2019 The Pharmacovigilance Training II Edition finalized on 10th May 2019, please contact us for more information about training courses After the successful first edition, PVpharm is organizing a face-to-face training in Madrid on 9-10 May 2019. Join us to learn about the latest updates! This training is - [PHARMACOVIGILANCE TRAINING III Edition](https://pvpharm.com/pharmacovigilance-training-iii-edition/) - PHARMACOVIGILANCE TRAINING III Edition Madrid & Online 30-31 May 2022 The Pharmacovigilance Training III Edition finalized on 31th May 2022, please contact us for more information about training courses After the successful previous editions, PVpharm is organizing a face-to-face training in Madrid on 30-31 May 2022. Don’t miss the III Edition!In addition, in this edition we - [cookies](https://pvpharm.com/cookies/) - BACKGROUNDIn accordance with Spanish regulations governing the use of cookies in relation to the Provision of Electronic Communications Services, set out in the Spanish Royal Decree Law 13/2012 of March 30, we inform you about the cookies used on the website of PV PHARM S.L (also the provider) and the reason for its use. 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