In less than six months – on 26 May 2021 – the Medical Devices Regulation (MDR) and the corresponding Swiss Medical Devices Ordinance (MedDO) will come into force. In our role as an industry association, we wish to provide advice and support with the webinar series titled «MDR Readiness Q&A».
On 26 May 2021 the Medical Devices Regulation (MDR) and the corresponding Swiss Medical Devices Ordinance (MedDO) will come into force. However, there is currently no indication that the Mutual Recognition Agreement (MRA) will be updated in the near future. The decision to implement measures to conform with the third country requirements must be taken by each company itself. In our role as an industry association, we wish to provide advice and support – and are therefore offering a webinar series titled «MDR Readiness Q&A». Use this opportunity to ask me and three renowned experts your questions directly.
Dates
17 December 2020 – 12.30h (English)
18 December 2020 – 12.30h (French)
18 December 2020 – 16.30h (German)
21 December 2020 – 12.30h (English)
From 12.30 – 13.30 h or 16.30 – 17.30 h
Choose your date and register now
Moderation
Dr. Daniel Delfosse, Head of Regulatory Affairs
