Pharmacovigilance
Build your professional skills in pharmacovigilance with our expert-led training programs. Gain in-depth knowledge of the legal framework, roles and responsibilities of the QPPV and the German Stufenplanbeauftragter, EudraVigilance reporting, audits and inspections, PSMF, GVP guidelines, Risk Management Plans (RMP) and Periodic Safety Update Reports (PSUR).
Thema
Dates
Format
Qualification Course: AI Management in the Pharmaceutical Industry
This qualification course is aimed at professionals and leaders in the pharmaceutical industry who already have basic prior knowledge of artificial intelligence.
13.10.2026 - 31.12.2027
Modulare Weiterbildung
Details
Qualification Course: Head of Pharmacovigilance
Within 2 years, you will complete three selected live training courses and one elective live training course on fixed dates. You will gain comprehensive knowledge for your responsibilities as Head of…
01.06.2026 - 31.12.2027
Modular Continuing Education
Details
Qualification Course: Qualified Person for Pharmacovigilance (QPPV)
Within 2 years, you will complete three live training courses on fixed dates and gain comprehensive knowledge for your responsibilities as a pharmacovigilance system professional. For newly appointed…
01.06.2026 - 31.12.2027
Modular Continuing Education
Details
ExpertFORUM Labelling
This online conference covers key EU regulatory developments shaping labelling in 2026, practical best practices for compliant day-to-day labelling, progress on ePI and QRD updates, and the latest AI…Language: English
19 - 20/11/2026
Online-Seminar
Details
The Pharmacovigilance System Master File (PSMF) in a Global Environment
This one-day online seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant local peculiarities worldwide.Language: English
04/03/2027
Online-Seminar
Details
Pharmacovigilance Inspection Readiness
This advanced one-day online course provides a practical framework for successfully managing pharmacovigilance inspections in Europe and globally, from long-term readiness planning through to CAPA…Language: English
22/02/2027
Online-Seminar
Details
Audit-Ready AI in Pharmacovigilance: Governance, Validation, and Documentation
This one-day advanced seminar uses a pharmacovigilance use case to demonstrate the governance, validation and risk-based control of AI across GxP-regulated environments.Language: English
03/02/2027
Online-Seminar
Details
The EU Qualified Person for Pharmacovigilance (EU QPPV)
This comprehensive two-day online course equips aspiring and practising QPPVs with the regulatory knowledge and practical skills needed for effective oversight and ongoing compliance.Language: English
17 - 18/02/2027
Online-Seminar
Details
An Introduction for Pharmacovigilance Managers
This intensive two-day online course provides a concise yet comprehensive overview of core pharmacovigilance activities, EU regulatory requirements, and their practical implementation.Language: English
Online-Seminar
Details
Pharmacovigilance Key Performance Indicators
In this compact one-day online course, you will learn how to use mandatory and optional KPIs to strengthen compliance and inspection readiness within your PV system.Language: English
28/09/2026
Online-Seminar
Details
Artificial Intelligence in Pharmacovigilance
This one-day online training explores practical AI applications in pharmacovigilance, including current use cases, hands-on applications of large language models, and the opportunities and limitations…Language: English
28/01/2027
Online-Seminar
Details
The GVP Refresher
The Good Pharmacovigilance Practices (GVP) Modules published by the European Medicines Agency (EMA) are the key reference for pharmacovigilance practice in Europe. This two-day online course offers a…Language: English
10 - 11/11/2026
Online-Seminar
Details
Masterclass: Local QPPV, EU QPPV, and Head of PV
Are you experienced in pharmacovigilance and looking for in-depth knowledge on managing a PV system and leading your team? Do you have specific questions about your role as responsible person? Then…Language: English
26/10/2026
Online-Seminar
Details
Pharmacovigilance Auditing
This compact, interactive 1.5-day online course equips you to independently plan and conduct pharmacovigilance audits in line with Good Pharmacovigilance Practices (GVP).Language: English
12 - 13/10/2026
Online-Seminar
Details
An Introduction for Pharmacovigilance Managers
ATTENTION NEW DATE. The seminar has been rescheduled from 7-8 to 8-9 October! This intensive two-day online course offers a concise yet comprehensive overview of all core elements of…Language: English
Online-Seminar
Details
Modern Risk Minimisation for Safety Professionals
This online seminar covers the regulatory requirements and practical implementation of (additional) risk minimisation measures ((a)RMM), from their design and selection to evaluation and ongoing…Language: English
04/12/2026
Online-Seminar
Details
Abonnement: PharmaFORUM Webcast International
Stay informed with updates from our global and local experts, who will provide the latest regulatory and legislative insights every two months. In 2026, topics will include CMC documentation,…Language: English
01/11/2026 - 31/10/2027
Abonnement
Details
Contact
We are happy to provide you with personal and individual advice.
Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.
Nadja Wolff
Conference Manager Healthcare
+49 6221 500-696
n.wolff@forum-institut.de