MDR readiness Q&A

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. 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». We will be happy to provide you with the recordings and the presentation.

Recording

Presentation by Daniel Delfosse

Q&A Session

Presentation

Moderation

Dr. Daniel Delfosse

Head of Regulatory Affairs

+41 31 330 97 74

E-Mail

Organisation

Angela D’Aranno

Project Assistant

+41 31 330 97 70

E-Mail

MDR Readiness Q&A
Experts

Bernhard Bichsel (ISS)
Bassil Akra (QUNIQUE)
Karin Schulze (SFL)
Marie Gaumet (ISS)
Michael Maier (Medidee)
Peter Studer (Confinis)
Jasminka Roth (Tao of Excellence)
Angelina Hakim (QUNIQUE)
Markus Wipf (Axxos)