Does the Falsified Medicines Directive lead to a European pack coding guideline?
22 April 2017 | By Johan Verhaeghe (Medicines for Europe)
The Directive on Falsified Medicines (FMD, or Directive 2011/62/EU amending Directive 2001/83/EC) and its supplementing Delegated Regulation (DR 2016/161) aim to improve patient safety by preventing falsified medicines from entering the legal supply chain...
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