Meet the EU MDR technical requirements for data
To help build public trust, the EU Medical Device Regulation (EU MDR) aims to increase patient safety and improve transparency of the business operations and supply chains of medical devices manufacturers.
Get ready for the challenging reforms set to cause major disruption to the medical devices industry. Learn how to prepare a cross-functional approach to implementing the requirements of the EU MDR, including production, marketing and supply chain management. Watch the recorded webinar to help you get ready with the OpenText™ EIM platform.
Director, life sciences strategy