If you’re just beginning your EU FMD compliance journey, this guide is for you. The EU Falsified Medicines Directive is full of detail and complexity—and you’ll need to know the ins and outs of the regulation long before the February 2019 compliance deadline.
Our experts break everything down for you so you can be informed—and ready to continue selling product across the EU.
Get the Tracelink eBook to learn:
- Details of EU FMD requirements and governance.
- How the law will impact manufacturers, parallel importers/distributors, packagers, and pharmacies.
- Essential information about the European Medicines Verification System.
- Key differences between EU FMD and U.S. DSCSA.
Download your complimentary copy now.
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