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European Falsified Medicines Directive
FMD Software Solutions for Wholesalers
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How does FMD affect the management of medicines?
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Since the directive requires a unique identifier (UI), prescription only medicines must have a product code that identifies its name, common name, the pharmaceutical form, strength, pack size and type, a serial and batch number, expiration date and if applicable the national reimbursement number. The UI has to be printed on the pack as a barcode and also be readable by a human.
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