What is FMD
The European Falsified Medicines Directive [2011/62/EU] (commonly known as FMD) has been brought in to address the issue of falsified medicines entering the legitimate medicines supply chain across Europe. Under the Directive, all new packs of prescription medicines placed from February 2019 onwards will have to bear two safety features: a unique identifier (UI) in the form of a 2D data matrix (barcode) and an anti-tampering device (ATD).
Wholesalers & Retailers have to adhere to the regulation by scanning the 2D barcodes, verify and decommission from their respective national databases depending on the nature of transaction
Pharmatotal is FMD ready
PharmaTotal FMD Features
With over 15 years of experience within the Pharmaceutical sector we are able to ensure that we provide a robust and targeted FMD solution to not only comply with the regulation but also assist in enhancing efficiency