How to Setup an Effective PV System in the UK and EU/EEA

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An essential guide to PV system implementation in the UK and EU/EEA.

Welcome to the replay of our insightful webinar, "QPPV Office: Ensuring Compliance and Safety in Pharmacovigilance". This session was packed with valuable information on the roles and responsibilities of the Qualified Person for Pharmacovigilance (QPPV), best practices for maintaining compliance, and strategies for ensuring drug safety.

Whether you are revisiting the webinar to deepen your understanding or watching it for the first time, you’ll find practical insights and expert advice that can help your organization excel in pharmacovigilance.

Have Questions? We're Here to Help!

If you have any questions or need further assistance regarding the topics covered in the webinar, our team of experts is here to help.

Speak with an Expert

Meet Our Experts

Thomas Chatzopoulos

Vice President, QPPV Office

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Susanna Heinonen

EU/EEA QPPV

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David Lough

Senior Pharmacovigilance Consultant, QPPV Office

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Thomas Chatzopoulos

Thomas Chatzopoulos brings over 25 years of Pharmacovigilance expertise, having held senior roles at leading pharmaceutical companies including Grünenthal, Novartis, and Boehringer Ingelheim. As Vice President of the QPPV Office at ProPharma, he oversees QPPV and LPPV activities, leveraging his extensive experience in setting up global PV systems and preparing them for audits and inspections.

Susanna Heinonen

Susanna Heinonen is a seasoned GxP professional with more than 14 years of experience in the pharmaceutical industry. She has a proven track record in setting up and monitoring GxP systems, and has worked in various consultancy and leadership roles. At ProPharma, Susanna applies her deep expertise in multinational projects, cross-functional collaboration, and vendor management.

David Lough

David has been working in Pharmacovigilance Consulting for the past 8 years and has held the roles of EU QPPV, UK QPPV and UK NCP. David is an expert on the creation and management of marketing authorisation holder PV systems. Within ProPharma, David is the PSMF SME and has been responsible for the coordination, creation and/or maintenance of around 30 client PSMFs. As the PSMF SME, David is often involved in client audits and inspections and has used this exposure to continuously improve and update ProPharma’s PSMF creation and maintenance process.