Joint Drug Information Association (DIA)/European Medicines Agency (EMA) Information Day on Post-Authorisation Studies (PAS)

This information day will take place on 5 June 2015 at the EMA premises in London. It will provide an overview of regulatory procedures, requirements and scientific guidelines on the conduct of both safety and efficacy studies, and explore the benefits of the European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP) in supporting stakeholders in the conduct of PAS for regulatory decision making.

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