Overview
This conference will take stock of where we stand in the EU on falsified medicines and paint the landscape of the global issue. The speakers will present the approaches of the Member States on the implementation of the new legislation, and the impact and achievements of the concerned stakeholders such as industry, patients, pharmacies and distributors who have worked independently and together to find solutions. The key messages of the meeting will be presented in a paper outlining the positive benefits until now and also the challenges yet to be addressed.
Please register for the event at TOPRA website.
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Program Committee
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Ursula Busse, PhD, MBA Head of Regulatory Affairs
Tigen Pharma SA, Switzerland -
Gerald W. Heddell Director, Inspection Enforcement & Standards Division
Medicines and Healthcare products Regulatory Agency (MHRA), United Kingdom -
Susanne Keitel, DrSc, RPh Director
European Directorate for the Quality of Medicines & Healthcare (EDQM), France -
Syed Qadri Lead Consultant
GENPACT Pharmalink, United Kingdom
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