Overview
New technologies, evolving regulatory expectations and increasingly complex global operating models are changing how pharmacovigilance systems are designed, managed and overseen. QPPVs must continue to meet today’s requirements while also preparing their organisations for what comes next.
This year, the UK National QPPV Forum will do more than deliver essential regulatory updates. We want to challenge participants to look ahead, question established approaches and consider what they would like to change about the future of pharmacovigilance in the UK.
Are current oversight models still fit for purpose? Could established ways of working become more proportionate and better aligned with global systems? What should good governance look like as AI and automation become part of everyday pharmacovigilance? And where could closer collaboration between regulators and industry turn shared challenges into practical solutions?
Program Committee
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Elspeth McIntosh, MBA, RN Director
Castle Pharmacovigilance Ltd, United Kingdom -
Louise Woodward, PhD UK QPPV and Local Safety Responsible
Roche Products Ltd, United Kingdom -
Helen Fiddes Head of Patient Safety, UK and Ireland
Bristol-Myers Squibb, United Kingdom -
Lauren East Head Pharmacovigilance and Medical Information / UK QPPV
Abbvie, United Kingdom -
Rory Littlebury Head of PVSO and QPPV Office
GlaxoSmithKline (GSK), United Kingdom -
Sophie Radicke, MSc Head of GPvP and Lead Senior Pharmacovigilance Inspector
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
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