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Matcher jeres virksomhed kravene til sporbar identifikation på yderemballagen?

The incidence of falsified, counterfeit or unauthorized medicine in the open market is increasing globally.

By 2016, the EU Falsified Medicines Directive (FMD), incorporating obligatory identification and authenticity features on the outer packaging, will become mandatory.

HSA Systems responds to the challenge with a unique, complete and fully integrated solution, which makes it easy for pharmaceutical manufacturers and contract packers to comply with the FMD.
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