In our weekly expert view piece, Mark De Simone, chief executive of Aegate, a company which operates a highly secure real-time system to verify the authenticity of medicines, examines the recently published Falsified Medicines Directive (FMD).
Europe stands on the brink of a new world of improved patient safety, increased pharmaceutical supply chain transparency and potential healthcare cost savings. All as the result of the new EU legislation – the Falsified Medicines Directive (FMD).
Ahead is a huge change management project for all members of the pharmaceutical supply chain - from the production of medicines through to the final delivery to patients.
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