With the upcoming EU Falsified Medicines Directive (FMD), the challenges of shipping drug product throughout Europe are increasing exponentially. Companies selling product in the EU have just two years to comply with the comprehensive regulations.
Proper knowledge and planning is absolutely essential to eliminate risk for your business. What’s required under the law? What have early adopters learned? Where should you begin?
Watch this on-demand webinar with Brian Daleiden and Caitlin Czulada where we will discuss:
Product and master data
Compliance reporting and verification
Partner and level 3 integration
The European hub
You’ll also hear insights based on real-world experiences of pharma companies already shipping serialized product in the EU using the TraceLink Life Sciences Cloud.
EU Falsified Medicines Directive: What to Know and Where to Start
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