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Getting Started: EU FMD Guide to Pharma Serialization

EU FMD compliance Infographic

If your company is part of the pharmaceutical supply chain in Europe, preparing for the EU Falsified Medicines Directive should now be a priority. The regulation presents considerable challenges and responsibilities—serialization, government reporting, verification—so understanding the requirements and knowing how to prepare for the February 2019 deadline is a must. 

Our latest infographic can get you started on the road to EU FMD compliance. It covers the regulations' essential facts, including which nations are affected—and which have a compliance grace period—what each supply chain company must do to comply, and other vital details about:

  • Which products can be grandfathered. 
  • The 2D DataMatrix code format. 
  • The specific data that must be uploaded and maintained. 

 

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Infographic EU FMD Compliance Global Compliance Regulatory/Compliance

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More Serialization and Compliance Resources

Can You Afford a Manual Approach to EU FMD Compliance?

Manual data upload through the EMVO portal is simple in concept, but preparing and maintaining that data can be a challenge for smaller companies.

The Impact of EU FMD on Pharmacy Workflow and Stock Management

View an infographic on how EU FMD changes hospital and pharmacy workflows.

What Are the 3 Major Requirements of EU FMD?

The EU Falsified Medicines Directive contains requirements for safety features and verification that details how companies must establish serialization and reporting.

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