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Holiday Inn London Kensington Forum

21 feb 2017 8:00 a.m. - 22 feb 2017 12:00 p.m.

97 Cromwell Road, London, SW7 4DN, United Kingdom

Post-Authorisation Studies

This course offers insight into EU legislation on PASS and PAES. Examples of PAS protocols as well as some examples of classic pitfalls in study conduct will be presented and discussed.

SESSION 1: INTRODUCTION TO PAS

Session Chair(s)

Michael  Busch-Sørensen

Michael Busch-Sørensen

Board Member

Danish Society for Pharmacoepidemiology, Denmark

Michael  Forstner, PHD, MPH, MSC

Michael Forstner, PHD, MPH, MSC

Managing Director, Head of Pharmacoepidemiology Practice

Mesa Laubela-Consulting, Switzerland

  • General introduction and practicalities
  • Relevant PASS legislation
    • Directives, regulations and delegated regulations
    • Relevant GVP modules
    • Templates
    • PASS Q&A
  • The link between Risk Management, risk minimization and PASS
  • How to handle imposed and non-imposed PAS (PASS & PAES) studies i.e. rules for reporting of milestones, amendments and safety data
  • ICSR/SUSAR reporting requirements according to GVP module VI

Speaker(s)

Michael  Forstner, PHD, MPH, MSC

INTRODUCTION TO PAS

Michael Forstner, PHD, MPH, MSC

Mesa Laubela-Consulting, Switzerland

Managing Director, Head of Pharmacoepidemiology Practice

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