Pharmacovigilance
Build your expertise in pharmacovigilance, drug safety and patient safety with practice-oriented training for all levels of experience.
Topics
- QPPV responsibilities
- case management and signal management
- benefit-risk assessment and risk management
- literature monitoring, medical writing and the PSMF
- quality management, compliance, audits/inspections, and vendor management
Unless stated otherwise, the focus is on EU regulations, GVP requirements, and relevant ICH guidelines, complemented by selected courses on global pharmacovigilance topics and country- or region-specific requirements.
If you are looking for a topic that is not currently included, please feel free to contact us. We also offer tailored in-house training solutions for companies.
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
Modular Continuing Education
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
Advanced Class: The Global Network of Local and Regional QPPVs
This advanced online course strengthens collaboration between QPPV Offices and national PV teams. Centred on inspection readiness, it shows how global and local functions work together effectively.Language: English
10/05/2027
Online-Seminar
Details
Quality Management in Pharmacovigilance Systems
This intensive one-day online course provides practical guidance on implementing the quality requirements of GVP Module I and on monitoring and optimising your pharmacovigilance system.Language: English
16/04/2027
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
03 - 04/05/2027
Online-Seminar
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 one-day advanced online course provides a practical framework for managing pharmacovigilance inspections in Europe and globally, from long-term readiness planning through to CAPA follow-up.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
08 - 09/03/2027
Online-Seminar
Details
Artificial Intelligence in Pharmacovigilance
This one-day up-to-date online training covers AI use cases in pharmacovigilance, practical LLM applications, and the opportunities and limitations of AI-supported PV workflows.Language: English
28/01/2027
Online-Seminar
Details
The GVP Refresher
This two-day online seminar offers an up-to-date refresher on Good Pharmacovigilance Practices (GVP), combining current regulatory insights with practical workshops on PV quality assurance.Language: English
10 - 11/11/2026
Online-Seminar
Details
Masterclass: Local QPPV, EU QPPV, and Head of PV
This one-day masterclass offers experienced experienced PV professionals practical insights into PV system management, leadership and inspection readiness, combined with high-level peer exchange.Language: English
26/10/2026
Online-Seminar
Details
Modern Risk Minimisation for Safety Professionals
This one-day advanced online course covers the regulatory requirements and practical implementation of (additional) risk-minimisation measures, from their selection through to their evaluation.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