The Falsified Medicines Directive: Five steps to compliance
Ahead of the Falsified Medicines Directive (FMD) coming into play in the European Union on February 9, Christian Taylor, Serialization Business Consultant at Zetes, provides his five-step plan to becoming FMD compliant in an Expert View piece.
The FMD 2011/62/EU aims to increase the security of the manufacturing process and delivery of medicines throughout Europe, providing greater protection for patients.
Organizations that have not yet become compliant must now act fast to ensure they don’t fall foul of the regulation. So, what can be done to make sure FMD compliance projects are completed in time and that the chosen solutions are robust enough to guarantee immediate compliance? This is a five-step plan to becoming FMD compliant:
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