This is what MedtecLIVE and MedTech Summit 2019 have to offer.
Implementing the provisions of the MDR continues to be one of the major topics of the industry. MedXregulation gives an overview of the current state of affairs at Notified Bodies, authorities and other key players and presents valuable information on post-market surveillance instruments and the impacts on OEM/PLM relations and supplier companies.
- Wednesday 22 May
- MDR: Potential Synergies when Applying for FDA
- Business Impact MDR & Best Practice of Implementation
- Navigating the EU MDR Requirements for Combination Products
- Artificial Intelligence Between Innovation, Standardization and Regulation
- Artificial Intelligence in Medical Devices – Requirements of a Notified Body
- Regulation of AI in Medical Products: to Find the Right Measure!