Swiss Medtech Webinar

Manufacturer and critical supplier in dialogue: Strategies for joint success


The MDR (Medical Device Regulation) is putting the business relationship between medical device manufacturers and critical suppliers to the test: not only do manufacturers have to fulfil new and extensive requirements, the role of the supplier has also changed significantly under the MDR. In this webinar, Marco Scicolone (Metecon GmbH Switzerland) will show you how to maintain successful cooperation through mutual support. To this end, we will translate the applicable regulatory requirements for manufacturers and suppliers using practical examples from a supplier's environment (Mawatec AG).
 

Target group

The webinar is aimed at medical device manufacturers and their suppliers as well as all interested players in the medical technology industry who want to know how cooperation between manufacturers and suppliers can succeed under the MDR. 


The entire event will be held in German, starting at 10:00 am and ending at 11:30 am. It is free of charge for members of Swiss Medtech and ASD. All others can register for a fee of CHF 60. Please send us your most urgent questions when you register.

Swiss Medtech Webinar
20th September 2024
in German

Webinar
10h00 – 11h30

Moderation

Dr. Daniel Delfosse

Vice Director

Head of Regulation & Innovation

+41 31 330 97 74

E-Mail

The event will be held in German, so the programme will also be in German.

Programm

10.00 – 10.10 h
Moderation und Einführung Swiss Medtech
→ Daniel Delfosse, Leiter Regulation & Innovation, Swiss Medtech
10.10 – 10.15 h
Einleitung Metecon
→ Marco Scicolone, Standortleitung Schweiz und Business Development, Metecon Schweiz GmbH
10.15 – 10.50 h
Präsentation Metecon
→ Katharina Thievessen, Prokuristin & Head of Operations, Metcon GmbH
10.50 – 11.30 h
Fragen und Diskussionsrunde
→ Teilnehmende

Recording (in German)

 

Organisation

Angela D’Aranno

Project Manager

+41 31 330 97 70

E-Mail

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