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).

Qualification Course: Head of Pharmacovigilance
- Modular training programme consisting of three selected seminars and one elective module for Heads of Pharmacovigilance -Learn the responsibilities and legal aspects of managing a PV system and…
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.Qualification Course: Qualified Person for Pharmacovigilance (QPPV)
- Modular training programme consisting of three selected seminars for Qualified Persons for Pharmacovigilance -Gain insight into the legal framework and core responsibilities of the Qualified…
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
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
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
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
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
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
Artificial Intelligence in Pharmacovigilance
This one-day online training explores regulatory foundations and practical AI applications in pharmacovigilance, including current use cases, hands-on applications of large language models, and the…Language: English
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
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
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
Pharmacovigilance Signal Management
This interactive two-day seminar covers the regulatory fundamentals of signal management and their practical implementation through PRAC case studies, using EudraVigilance, programmable data analysis,…Language: English
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
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
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