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Virtual Event

2020年11月02日 (月) 午後 1:00 - 2020年11月04日 (水) 午後 4:25

(Central Europe Standard Time)

4051 Basel, Switzerland

Pharmacovigilance Strategies Workshop

Session 8: Risk Minimisation Measures and Safety Communication

Session Chair(s)

Shahin  Kauser

Shahin Kauser

Leading Senior Scientific Assessor, MHRA, United Kingdom

Maarten  Lagendijk, MSC

Maarten Lagendijk, MSC

Deputy EU QPPV, MSD, Netherlands

Revision 2, of GVP Module XVI, provide guidance use of additional risk minimisation measures including the selection tools and their evaluation of their effectiveness. Additional risk minimisation measures include educational materials, controlled access programmes and controlled distribution systems. This session will explore some examples of such measures and the measurement of effectiveness to help stimulate discussion. There will be perspectives from Industry and the UK regulatory agency. In addition to hearing from the speakers, attendees will be encouraged to share their experience as part of the Panel Discussion.

Speaker(s)

Maarten  Lagendijk, MSC

Maarten Lagendijk, MSC

Deputy EU QPPV, MSD, Netherlands

Additional Risk Minimisation Measures (aRMM): Why do they matter?

Jan  Petracek, MD, MSC

Jan Petracek, MD, MSC

CEO, iVigee Services a.s., Czech Republic

Running Risk Minimisation Programs – Lessons Learned

Shahin  Kauser

Shahin Kauser

Leading Senior Scientific Assessor, MHRA, United Kingdom

Controlled Access Programmes

Inge  Zomerdijk, MSC

Inge Zomerdijk, MSC

Pharmacovigilance Assessor, Medicines Evaluation Board (MEB), Netherlands

Measuring the Effectiveness of aRMM

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