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FMD overview for pharma suppliers

Wednesday 4 April 2018

10:30 AM to 11:00 AM

United Kingdom

Member price: Free per person

Non-Member price: Free per person

Overview

An understanding of GS1 standards will be crucial in complying with the Falsified Medicines Directive (FMD) which is currently being implemented across Europe.

As a pharmaceutical manufacturer, this interactive webinar will help you with the basics to ensure your implementation project starts off on the right foot.

Who should attend?

This is an introductory webinar, perfect for those just starting out on their compliance journey or undertaking a new area of responsibility.

If you require a more detailed understanding in order to implement GS1 standards for medicines, come along to next month’s public course or have it delivered in-house.

Learning outcomes

By the end the webinar, you will understand:

  • Which GS1 standards will help you meet the FMD requirements
  • Timelines involved
  • Next steps
  • The tools and services available to support your implementation

Plus you'll have the opportunity to ask one of our experts questions specific to your business.