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Securing the Supply Chain: How to Tackle the Challenges
Session Chair(s)
Susanne Keitel, DRSc, RPh
Director, European Directorate for the Quality of Medicines & Healthcare (EDQM), France
This session will look into the status and next steps with regard to the implementation of the EU Falsified Medicines Directive with a focus on the new rules on safety features, which should be published in early 2016. Participants will also hear about the challenges the implementation poses to industry, and how they may be addressed. Work within the EU is complemented by projects and initiatives at the EDQM, with an aim to secure medicinal product quality and supply chains.
Speaker(s)
Patrizia Tosetti, PhD
Policy Officer, European Commission - DG Health and Food Safety, Belgium
The Implementation of the Falsified Medicines Directive – What’s New?
Stephan Roenninger, DRSc
Director, Quality Compliance External Affairs , Amgen (Europe) GmbH, Switzerland
Practical Implementation of the Falsified Medicines Directive: A Challenge for Industry?
Susanne Keitel, DRSc, RPh
Director, European Directorate for the Quality of Medicines & Healthcare (EDQM), France
The Holistic Strategy of the EDQM to Secure the Supply of Medicines to Patients
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