The Falsified Medicines Directive (FMD) 2011/62/EU, which comes into full force on 9 February 2019, aims to increase the security of the manufacturing process and delivery of medicines throughout Europe, providing greater protection for patients.
Organisations 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? Christian Taylor, serialisation business consultant at Zetes, provides his five-step plan to becoming FMD compliant.