Adents Blog EU FMD : new FAQ document gives guidance on safety features for medicinal products

The European Commission has recently released Version 16 of their QUESTIONS AND ANSWERS regarding safety features for medicinal products for human use compliant with EU Falsified Medicines Directive (EU FMD) 2011/62/EU. Following the high number of alerts triggered when medicines were scanned prior to dispensation, the new version of the FAQS includes recommendations on the […] The post EU FMD : new FAQ document gives guidance on safety features for medicinal products appeared first on Adents English.