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Fighting Falsified Medicines in Europe –Supply Chain Digitalisation for the Benefit of Patients: Are You Ready?
Session Chair(s)
Andreas Walter
Director General
European Medicines Verification Organisation, Belgium
The FMD comes into force on 9th February 2019. This session will discuss a few of the practical issues which may come up during the go-live phase, including the current state of play, the use of the data by the supervising authority, the enforcement of the rules and the handling of alerts in the system.
Speaker(s)
Legislative Framework
Agnes Mathieu-Mendes, RPh
European Commission, Belgium
Deputy Head of Unit
State of the EMVS
Andreas Walter
European Medicines Verification Organisation, Belgium
Director General
Case Study
Belen Escribano Romero, PharmD, MPA
AEMPS, Spain
Head of Department, Pharmaceutical Inspection and Enforcement
Case Study
Philippe De Buck, MPharm
FAGG-AFMPS, Belgium
Head of Authorisations
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