Implementation of the new Regulations (MDR, IVDR), Clinical investigations, Medical device with drug substance
This evening is an ideal opportunity to discuss the new medical device regulations MDR and IVDR which will be fully implemented from 26 May 2021 respectively. 26 May 2022. How is the work at the Medical Products Agency changed and how does a company prepare? How will they affect clinical investigations of medical devices? And what is the consultation for a medical device with a drug substance and MDCG 2020-12? Open to anyone who works with and is interested in regulatory for medicines and medical devices. The meeting online due to covid-19.
21 October 2020, 18.30-21.00
TOPRA in Sweden - Medical Devices MPA 21Okt2020 Uppsala 201013 - EN translation.pdf (141.9 KB)