2025-11-21 2025-11-21 , online online, 3,600 € zzgl. MwSt. Qualification Course: Qualified Person for Pharmacovigilance (QPPV)

- Combination of three selected seminars - With this qualification course, you will first gain insight into the legal aspects and general responsibilities of the Qualified Person for Pharmacovigilance (QPPV). You will then deepen your professional and practical knowledge to perform your role more effectively.

Topics
    Your three training courses:
  • The EU Qualified Person for Pharmacovigilance (EU QPPV)
  • Within two days, learn the responsibilities and legal aspects of managing the PV system and deepen your practical knowledge through integrated workshops.
  • Advanced Class: The Global Network of Local and Regional QPPVs
  • Optimise communication and cooperation between local, regional, and global safety officers by preparing for an upcoming global PV inspection.
  • Master Class: Local QPPV, EU QPPV, and Head of PV
  • Enhance your detailed knowledge of typical challenges such as SOPs, deviations, stakeholder management, or findings and recalls.


Who should attend
This qualification course is aimed at experienced pharmacovigilance staff who currently hold or will in future take on the position of EU QPPV.

The seminars are designed to complement your professional role. Participants are encouraged to actively bring in specific problems or questions from their daily work.
Aims and objectives
Have you already been working in drug safety for some time and now wish to take the next step in your career as the responsible person for pharmacovigilance? As a National Safety Officer and/or QPPV, you bear responsibility for the PV system and must maintain oversight and control. Book our combined package and acquire both theoretical and practical knowledge on leading the PV system.

About the concept: You will take part in three live online training sessions within 24 months. These take place on fixed dates. Further information and upcoming dates for each seminar can be found below and on the respective event page.
Your benefit

  • Advance your career with a programme tailored to your professional needs.
  • Save time and rely on the right seminar package designed for your role.
  • For each course, you will receive a certificate of attendance. In addition, you have the opportunity to complete an online learning assessment with certification. This extra certificate serves as personal proof of competence and provides valuable support during inspections.
  • To ensure that what you learn can be applied directly to your daily work, each seminar includes practical exercises, workshops, and dedicated time for discussion.
After completing the training sessions and the learning assessments, you will receive the recognised FORUM certificate "Qualified Person for Pharmacovigilance (QPPV)".

Qualification course - Qualified Person for Pharmacovigilance

Qualification Course: Qualified Person for Pharmacovigilance (QPPV)

Modular training of 3 training courses for (future) responsible persons of the PV system

Benefits
  • 3 live online training sessions
  • Responsible management of the PV system
  • Save up to 25% compared with individual bookings
  • Certified to ISO 9001 and ISO 21001 standards

Webcode 60012061

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Termin

01/01/2025 - 31/12/2026

01/01/2025 - 31/12/2026

Zeitraum

You may begin the qualification programme with any seminar. We recommend beginning with the seminar "The EU Qualified Person for Pharmacovigilance (EU QPPV)". The modules take place live on fixed dates, are not available as recordings, and should be completed within 24 months.

You may begin the qualification programme with any seminar. We recommend beginning with the seminar "The EU Qualified Person for Pharmacovigilance (EU QPPV)". The modules take place live on fixed dates, are not available as recordings, and should be completed within 24 months.
Veranstaltungsort

online

online

Gebühr
Your contact

Nadja Wolff
Conference Manager

+49 6221 500-696
n.wolff@forum-institut.de

Details

- Combination of three selected seminars - With this qualification course, you will first gain insight into the legal aspects and general responsibilities of the Qualified Person for Pharmacovigilance (QPPV). You will then deepen your professional and practical knowledge to perform your role more effectively.

Topics

    Your three training courses:
  • The EU Qualified Person for Pharmacovigilance (EU QPPV)
  • Within two days, learn the responsibilities and legal aspects of managing the PV system and deepen your practical knowledge through integrated workshops.
  • Advanced Class: The Global Network of Local and Regional QPPVs
  • Optimise communication and cooperation between local, regional, and global safety officers by preparing for an upcoming global PV inspection.
  • Master Class: Local QPPV, EU QPPV, and Head of PV
  • Enhance your detailed knowledge of typical challenges such as SOPs, deviations, stakeholder management, or findings and recalls.


Who should attend
This qualification course is aimed at experienced pharmacovigilance staff who currently hold or will in future take on the position of EU QPPV.

The seminars are designed to complement your professional role. Participants are encouraged to actively bring in specific problems or questions from their daily work.

Aims and objectives

Have you already been working in drug safety for some time and now wish to take the next step in your career as the responsible person for pharmacovigilance? As a National Safety Officer and/or QPPV, you bear responsibility for the PV system and must maintain oversight and control. Book our combined package and acquire both theoretical and practical knowledge on leading the PV system.

About the concept: You will take part in three live online training sessions within 24 months. These take place on fixed dates. Further information and upcoming dates for each seminar can be found below and on the respective event page.

Your benefit

  • Advance your career with a programme tailored to your professional needs.
  • Save time and rely on the right seminar package designed for your role.
  • For each course, you will receive a certificate of attendance. In addition, you have the opportunity to complete an online learning assessment with certification. This extra certificate serves as personal proof of competence and provides valuable support during inspections.
  • To ensure that what you learn can be applied directly to your daily work, each seminar includes practical exercises, workshops, and dedicated time for discussion.
After completing the training sessions and the learning assessments, you will receive the recognised FORUM certificate "Qualified Person for Pharmacovigilance (QPPV)".

The Concept

How to customise your qualification course

You will take part in four live training sessions (modules) within 24 months. These take place on fixed dates. Information and upcoming dates for each seminar can be found on the respective event page. The three compulsory modules provide you with a comprehensive overview of the responsibilities and essential tasks of a Head of Pharmacovigilance. An additional elective module allows you to choose a topic according to your personal interests.

You may begin the qualification programme with any seminar. Please note, that only the module "Qualified Person for Pharmacovigilance (EU QPPV)" covers the regulatory foundations of the role. The other two modules focus on specific tasks and practical duties associated with the position. For participants with little prior familiarity with these responsibilities, we recommend starting with this module.

Our compulsory modules are offered at least once a year. If you are unable to attend on a specific date, or if your preferred seminar is not yet available online, this is not a problem. Simply book the qualification course, and we will arrange the seminar dates with you individually. If you have any questions or would like personal support in selecting or booking your modules, please feel free to contact me directly at n.wolff@forum-institut.de or by telephone at 06221 500-696.

The benefits for your employer

  • Your employer invests in high-quality and well-prepared knowledge transfer, ensuring a solid foundation of expertise within the company.
  • You are up to date and contribute current know-how to the organisation.
  • Benefit from the carefully selected seminar package and approve four training sessions in one process.
  • Your employer saves up to 25% compared with individual seminar bookings.

3 compulsory modules (offered annually)

Advanced class: The Global Network of Local and Regional QPPVs

Are you a QPPV, local Safety Officer, or part of a QPPV office within an international MAH? Looking for a targeted train...

11.12.2025
Details

The EU Qualified Person for Pharmacovigilance (EU QPPV)

This two-day course equips new or in future QPPVs with the fundamentals of EU pharmacovigilance legislation, QPPV respon...

13. - 14.01.2026
Details