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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)
The Implementation of the Falsified Medicines Directive – What’s New?
Patrizia Tosetti, PhD
European Commission - DG Health and Food Safety, Belgium
Policy Officer
Practical Implementation of the Falsified Medicines Directive: A Challenge for Industry?
Stephan Roenninger, DrSc
Amgen (Europe) GmbH, Switzerland
Director, Quality External Affairs
The Holistic Strategy of the EDQM to Secure the Supply of Medicines to Patients
Susanne Keitel, DrSc, RPh
European Directorate for the Quality of Medicines & Healthcare (EDQM), France
Director
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