Global Forum for Qualified Persons for Pharmacovigilance (QPPV)

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Overview

The DIA Global QPPV Forum is a must-attend conference for anyone involved in pharmacovigilance. With a focus on the most pressing issues facing the industry today, this year's topics include global QPPV challenges, trends requiring QPPV awareness, and the impact of modern technology on the field. In addition, we will continue our popular 'QPPV talks' - quick, inpirational sessions that provide practical insight into real-world cases.

With input from regulators and industry leaders from around the world, this conference promises to provide valuable insights into the most pressing issues facing QPPVs today - and don't forget our 'Hot Topics' session!

So join us at the DIA Global QPPV Forum to network with peers, gain valuable insights, and stay ahead of the curve in the ever-evolving role.

Why should you attend this conference?

Angela Van der Salm, Director Pharmacovigilance, Managing Partner, DADA Consultancy, Netherlands

“For me, the annual QPPV forum is the place to meet my colleagues in the field that have just joined or that have been in the QPPV role for decades, all sharing experiences and best-practices in that particular role that is at the core of the pharmacovigilance system. Every year, the agenda includes topics on the further globalization of the role, current developments in (guidance for) legislation and is a platform for interaction between regulators and industry. I am thrilled that this year is in a live setting again and am very much looking forward to meet you in person!”

Free Session | Management of Shortages and the QPPV involvement

This session provides valuable insights and practical solutions shared by industry and regulators as well as clarify the expectations from the MHRA, including the role of the QPPV in this matter.

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Exhibits

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Short Course or Primer

To keep you at the forefront.

Nov 07, 2023

Pre-conference Workshop 1: Introduction to the Role of QPPVs
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Nov 07, 2023

Pre-conference Workshop 2: Globalisation of PSMF
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Who should attend?

Global QPPVs/ Deputies
Regulators
Pharmacovigilance Consultants
Directors of Pharmacovigilance Oversight and Standards
Drug Safety Managers/Leaders
Auditors
Medical and Regulatory Affairs Experts
Aspiring PV Specialists/QPPVs

Program Committee

Gemma Jimenez Sese • Patient Safety Director, EU QPPV
Almirall, S.A., Spain
Magnus Ysander, MD • EU & UK QPPV & Head Pharmacovigilance Excellence
AstraZeneca, Sweden
Angela Van Der Salm, PhD, MSc • Director PV, Managing partner
DADA Consultancy B.V., Netherlands
Shahinaz Badr • Pharmacovigilance Consultant and PVQA Auditor - EMEA
Pharma Quality Europe, United Arab Emirates
Vicki Edwards, RPh • Vice President, Pharmacovigilance Excellence and International QPPV
Abbvie, United Kingdom
Maarten Lagendijk, MSc • Deputy EU QPPV
MSD, Netherlands
Elspeth McIntosh, MBA, RN • Director
Castle Pharmacovigilance Ltd, United Kingdom
Katarzyna Swiderek, MPharm, RPh • Director, Safety Evaluation Risk Management (SERM)
GlaxoSmithKline, Poland
Kiernan Trevett, MSc • Principal Quality Lead, PDQ Quality Assurance Process GVP
Roche, United Kingdom
Claire Longman, MSc • Expert Pharmacovigilance Inspector
Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom
Willemijn van der Spuij, MSc • Executive Director, WorldWide Patient Safety International, Europe
Switzerland

Contact us

Registration Questions?

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+41 61 225 51 51

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