UDI Expert Talk: How to organize the compliant implementation of the MDR? What do I have to do by when? From gap assessment to postponed deadlines

Our new online expert series "UDI Talk" offers a forum for a variety of topics around the UDI marking of medical devices. With regard to the MDR (European Medical Device Regulation), which will be in force from May 2021, we'll discuss current requirements and answer questions.

The topic of our first UDI Talk on June 9th is:

UDI and MDR: What do I have to implement by when? How do I organize the implementation according to the regulations? From gap assessment to the current postponement of the MDR transition deadlines

Your hosts Christian Söhner (FOBA Laser) and Michael Galliker (Regulatory Globe) will discuss:

• how companies can approach the implementation of the UDI according to the MDR (keyword "gap assessment")
• the relevant MDR regulations for direct part marking
• possible adjustments to the deadlines due to the latest MDR postponement
• the technical options for a UDI direct marking

Current developments are discussed promptly. Further topics are also discussed at the suggestion of the participants.