Why is UDI strategy so important?
The unique device identification initiative for medical devices and in vitro diagnostic medical devices is now an international hot topic and how you, as a manufacturer, respond will affect your bottom line in the coming years. Regulatory UDI requirements started with the US, spread to the European Union, and are now emerging in South Korea, Saudi Arabia, China and elsewhere. In parallel, your commercial business partners are starting to revise their contracts to specify UDI be placed on products and be included in electronically published product catalogs. For our valued customers, this webinar will focus on answering questions you may have about global regulatory submissions, starting with EU MDR. We will also review flexible solutions for UDI data management with options for implementing a stand-alone or integrated Data Hub Model with SingleSource™ for Medical Devices. Join medical device data experts from Reed Tech for a focused discussion on our implementation and phased plans for the EU Medical Device Regulation (MDR) UDI submission deadline of May 2020.
Webinar Replay (originally recorded: Thursday, March 28)
Who should attend?
- Unique Device Identification Team Members
- Global Strategy Business Managers
- Regulatory Affairs/Operation Leaders
- Product Managers and Business Analysts
- Manufacturing, Operations, and Supply Chain Leaders
- Quality Leaders
- Medical Device IT Support
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