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Content:

The course will take you through classification,
conformity assessment, the General Safety and Performance requirements as well as the specific regulatory requirements for clinical data, technical documentation,
economic operators, post-market surveillance and postmarket clinical follow-up.

Agenda Download here:

Agenda MDR.pdf (327.55KB)
Agenda MDR.pdf (327.55KB)

 

 

Package and Fees:

Certificates

Trainings Materials PDF and Hardcopy

Catering

CHF 700 excl.taxes

Group of Participants:

Medical Device Manufacturers

Importers, Distributors, Authorized Representative

Attendees

Reduction

3 to 5 Attendees

20% off

6 to 10 Attendees

25% off