The European Federation of Pharmaceutical Industries and Associations (EFPIA) has announced the official launch of the tendering process for key components of its European Medicines Verification System (EMVS) as of April 5, 2012.
The EFPIA plans to prove the efficiency and to demonstrate the viability of the EMVS through real-life implementation ahead of the publication of the European Commission’s Delegated Act on Safety Features (expected by 2014). The stakeholder-governed solution proposed by the EFPIA and its partners in the pharmaceutical supply chain is indeed likely to constitute the key solution for future implementation of the Falsified Medicines Directive.
The EMVS will consist of the following key components:
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