Date & Time
- from
- Wed/Dec/202509:00 am
- until
- Wed/Dec/202514:00 pm
- duration
- 5hours
Contents:
EU legal system for medical devices and IVDs
Medical Device Regulation (MDR and IVDR)
Medical Products Implementation Act (MPDG)
Medical Devices Operator Ordinance (MPBetreibV)
How does a product become a medical device/IVD?
Medical device consultant:in (MPDG)
Collaboration with the PRRC (MDR and IVDR) & Market Surveillance/PMS (MDR and IVDR)
Referent:in : Cornelius Weber and Dr. Katja Krempler
Costs: 250€ Members, 300€ non-members (net)
The above texts, or parts thereof, were automatically translated from the original language text using a translation system (DeepL API).
Despite careful machine processing, translation errors cannot be ruled out.