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.


Presentation by Daniel Delfosse

Q&A Session



Dr. Daniel Delfosse

Vice Director

Head of Regulation & Innovation

+41 31 330 97 74

+41 79 308 80 76



Angela D’Aranno

Project Manager

+41 31 330 97 70


MDR Readiness Q&A

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)