European Union Falsified Medicines Directive
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How Do I Prepare Product Master Data for EU FMD?
Learn what product master data you need to upload to the European Hub under EU FMD, and how to go about preparing it.
Case Study: Mithra | Serializing Across Multiple Business Cases
Learn how Mithra used a multidisciplinary approach for a successful EU FMD go-live.
Case Study: Merck | Driving Operational Excellence for EU FMD
See how Merck ensured a smooth implementation for EU FMD compliance.
Case Study: Medreich | Anti-Tampering and EU FMD
Learn how Medreich designed an EU FMD-compliant label to work with anti-tampering devices.
Case Study: Medreich | EU FMD from Project Plan to Post Implementation
See how Medreich and TraceLink collaborated to achieve EU FMD compliance.
Case Study: Ferrer | Building a Master Data Strategy for EU FMD
Learn how Ferrer worked with TraceLink to manage its master data for EU FMD compliance.
Getting Started: EU FMD Guide to Pharma Serialization
Get started with understanding EU FMD regulations and the serialization challenges ahead, with this introductory infographic guide.
Serialization, Onboarding Partnerships & the Hub under EU FMD
Learn from use cases that explore hub connectivity, onboarding & implementation timelines to meet compliance by February 2019.
50 Must-Know Terms to Achieve EU FMD Compliance
Learn the technical, legal, and industry terms you need to successfully prepare your company for EU FMD.
Building for EU FMD - 5 Serialization Leaders Share How to Prepare
See how experts have overcome roadblocks as they implement Level 1-5 solutions for EU FMD serialization.
Almirall and TraceLink: Committed to Quality and Innovation
Hear the Almirall team explain how they achieved FMD compliance with TraceLink.
Working with Contract Partners: The Actelion-Allpack Collaboration
Swiss pharma company Actelion and Allpack, a contract packager, discuss how they worked together towards serialization.