2025-08-30 2025-08-30 , online online, 4,500 € plus tax Qualification Course: Head of Pharmacovigilance

Combined offer of three compulsory seminars plus one elective module for (future) Heads of the Pharmacovigilance Department - learn the responsibilities and legal aspects of managing a PV system and its staff, and select an elective module according to your individual interests.

Topics
    About the concept:
    Within 24 months, you will take part in four live training sessions (modules). These take place on fixed dates. Three of these modules (compulsory modules) are already selected for you. One additional module (elective) can be chosen freely according to your personal area of interest. Three compulsory modules:
  • The EU Qualified Person for Pharmacovigilance (EU QPPV)
  • Pharmacovigilance Key Performance Indicators
  • Master Class: Local QPPV, EU QPPV, and Head of PV
    • One additional elective module:
  • Outsourcing and Vendor Management in Pharmacovigilance
  • The Pharmacovigilance System Master File (PSMF) in a Global Environment
  • RMP and PSUR in life-cycle management: An art, not a miracle
  • Global Pharmacovigilance Inspection Readiness
Aims and objectives
Have you been working in pharmacovigilance for some time and now wish to take the next step in your career as Head of the Pharmacovigilance Department? Secure our combined package and gain both theoretical and practical knowledge on leading a PV department.

The EU Qualified Person for Pharmacovigilance (EU QPPV)
  • Whether you hold the role of QPPV yourself, you must understand the responsibilities and legal aspects of managing a PV system.
Pharmacovigilance Key Performance Indicators
  • Effective quality assurance in the pharmacovigilance department is essential. Deepen your knowledge and manage your department using the right KPIs for your organisation.
Master Class: Local QPPV, EU QPPV, and Head of PV
  • Benefit from the decades of experience of our expert team and enhance your detailed knowledge on managing a PV system and its staff.
Who should attend

This qualification course is designed for experienced pharmacovigilance professionals who currently hold or intend to assume leadership of a pharmacovigilance department.

The seminars are practice-oriented and designed to complement your professional life. Participants are encouraged to actively contribute their own questions and real-life challenges from their daily work.

Upon successful completion, you will receive a recognised certificate with the title Head of Pharmacovigilance.

Qualification course - Head of Pharmacovigilance

Qualification Course: Head of Pharmacovigilance

Modular qualification course for (future) Heads of the Pharmacovigilance Department

Benefits
  • 4 live online training sessions
  • Experts with decades of PV experience
  • Responsible management of the PV department
  • Save up to 25% compared with individual bookings

Webcode 10044

Book now

JETZT Buchen

Everything at a glance

Appointment

01/01/-31/12/2025

01/01/-31/12/2025

Period

You can start the qualification course with any of the seminars. Please note that the modules take place on fixed dates live online and are not available as recordings. The seminars should be completed within 24 months.

You can start the qualification course with any of the seminars. Please note that the modules take place on fixed dates live online and are not available as recordings. The seminars should be completed within 24 months.
Venue

online

online

Downloads
Fee

Event - 4,500 € plus tax
The fee includes comprehensive course material for download, learning assessments, a certificate after each module, and a final overall certificate. Access to the Learning Space and technical support, including a pre-meeting session, are provided.

Event - 4,500 € plus tax
The fee includes comprehensive course material for download, learning assessments, a certificate after each module, and a final overall certificate. Access to the Learning Space and technical support, including a pre-meeting session, are provided.

Book now

Your contact

Nadja Wolff
Conference Manager

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

Details

Combined offer of three compulsory seminars plus one elective module for (future) Heads of the Pharmacovigilance Department - learn the responsibilities and legal aspects of managing a PV system and its staff, and select an elective module according to your individual interests.

Topics

    About the concept:
    Within 24 months, you will take part in four live training sessions (modules). These take place on fixed dates. Three of these modules (compulsory modules) are already selected for you. One additional module (elective) can be chosen freely according to your personal area of interest. Three compulsory modules:
  • The EU Qualified Person for Pharmacovigilance (EU QPPV)
  • Pharmacovigilance Key Performance Indicators
  • Master Class: Local QPPV, EU QPPV, and Head of PV
    • One additional elective module:
  • Outsourcing and Vendor Management in Pharmacovigilance
  • The Pharmacovigilance System Master File (PSMF) in a Global Environment
  • RMP and PSUR in life-cycle management: An art, not a miracle
  • Global Pharmacovigilance Inspection Readiness

Aims and objectives

Have you been working in pharmacovigilance for some time and now wish to take the next step in your career as Head of the Pharmacovigilance Department? Secure our combined package and gain both theoretical and practical knowledge on leading a PV department.

The EU Qualified Person for Pharmacovigilance (EU QPPV)

  • Whether you hold the role of QPPV yourself, you must understand the responsibilities and legal aspects of managing a PV system.
Pharmacovigilance Key Performance Indicators
  • Effective quality assurance in the pharmacovigilance department is essential. Deepen your knowledge and manage your department using the right KPIs for your organisation.
Master Class: Local QPPV, EU QPPV, and Head of PV
  • Benefit from the decades of experience of our expert team and enhance your detailed knowledge on managing a PV system and its staff.

Who should attend

This qualification course is designed for experienced pharmacovigilance professionals who currently hold or intend to assume leadership of a pharmacovigilance department.

The seminars are practice-oriented and designed to complement your professional life. Participants are encouraged to actively contribute their own questions and real-life challenges from their daily work.

Upon successful completion, you will receive a recognised certificate with the title Head of Pharmacovigilance.

Further Information

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.

To book the course, please contact me directly at n.wolff@forum-institut.de or by telephone at 06221 500-696.

Your personal benefits

  • Tailor your qualification precisely to your professional environment.
  • Save time and rely on the right training package for your career.
  • To support the practical transfer of knowledge into your daily work, each seminar includes exercises, workshops, case studies, and time for discussion.
  • After completing the training sessions and the learning assessments, you will receive a recognised FORUM certificate of successful qualification as Head of Pharmacovigilance.

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.

One additional elective module

Global Pharmacovigilance Inspection Readiness

Learn how to prepare your pharmacovigilance system in Germany, Europe and worldwide for an upcoming inspection in this o...

02.02.2026,
Details

RMP and PSUR in lifecycle management: An art, not a miracle

Do you already have a good understanding of PSUR and RMP including risk minimisation measures and would like to deepen, ...

29.01.2026,
Details
The Pharmacovigilance System Master File (PSMF) in a Global Environment

This online-seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant lo...

18.09.2025,
Details

Three compulsory modules

The EU Qualified Person for Pharmacovigilance (EU QPPV)

This two-day course equips beginners with the fundamentals of EU pharmacovigilance legislation, QPPV responsibilities, a...

Details
Online-Seminar
Pharmacovigilance Key Performance Indicators

Are you involved in the implementation and ongoing adaptation of the PV system? In this online course you will learn how...

Details
Online-Seminar
Masterclass: Local QPPV, EU QPPV, and Head of PV

Attention: Date change from 25 to 26 September 2025 - Are you experienced in pharmacovigilance and looking for...

Details
Online-Seminar