Understanding EUDAMED, Global Requirements and GDSN
November 19, 2019 12:00 pm – November 12, 2019 1:00 pm (EDT), Webinar

As we go into the next decade, most medical device manufacturers are planning for a future that includes a global outlook. Unique Device Identification (UDI) for medical devices and in vitro diagnostic medical devices are anticipated to carry UDI regulatory requirements expanding to multiple regions and channels. Additionally, many trading partners now require structured product data through standard communication networks (GDSN) that can be shared across departments and geographies. 

Attendees will learn:

  • How does Reed Tech and 1WorldSync work together to offer data submission/publishing solutions?
  • What are the dataflow options for reporting regulatory and commercial data to downstream users? 
  • The GS1 GTIN standard and the GDSN data publication process
  • The FDA deadline for Class I devices Sept 24, 2020 and an update on EUDAMED delay
  • The advantages of a comprehensive, global strategy for UDI compliance and syndication of data

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