Following the success of the RMD Conferences in Prague 2016, Berlin 2017, and Brussels in 2018 and 2019, the 5th EAAR Annual Conference on New Medical Device Regulations (RMD 2021) will be held as a ‘virtual’ event on 26/27 January 2021.

The Conference will give delegates the opportunity to gain a better understanding of the implementation of the new European regulations on medical devices, as new guidance documents are issued, and compliance expectations become clearer. The application date of the Medical Device Regulation (MDR, 2017/745) is only a few months away, so it is important for device manufacturers to keep up-to-date with the fast evolving compliance scene.

Speaking at 15:30 CET on the first day will be Maria E. Donawa, M.D., President of Donawa Lifescience, who will be presenting on the topic ‘Best Methods for Using ISO 14155: 2020 to Comply with MDR Clinical Study Requirements’. Dr. Donawa will be discussing the parts of ISO 14155:2020 that can be particularly helpful in ensuring compliance with MDR clinical investigation requirements.

Also, speaking on the second day, will be Gavia Taan from MHRA, who will provide an update on the UK medical device regulations post-Brexit.

For further details, please visit the RMD 2021 website.