EU Falsified Medicines Directive - What to Know and Where to Start
Original webcast: March 22, 2017
The countdown continues. We're now less than two years away from the EU Falsified Medicines Directive (FMD), one of the most significant changes the European pharmaceutical supply chain has ever experienced. How much do you and your colleagues now about the EU FMD requirements? Serialization, required by the regulation, is an immense challenge—much more than just putting a 2D DataMatrix on every package. It involves your entire operation, including your trade partners. If you haven't yet begun preparations, now's the time to start—and we can help.
Watch this free on-demand webinar to learn essential information about EU FMD, understand how it will affect your business, and hear what companies who are already live in the EU have experienced.
- What EU FMD implementation looks like, and who should be involved.
- How to manage integrations with your partners, and what questions to ask them.
- How to create your serialization timeline toward February 2019 compliance.