The main responsibilities are the ones mentioned on Article 15 of the EU MDR 2017/745:
Conformity of the product device to the Medical Device Regulation and Quality Management System
Conformity of the Technical Documentation and EU Declaration of conformity
Compliance with Post-Market Surveillance (PMS) following Article 10(10)
For Investigational devices: Issuance of a signed statement (Annex XV Chapter II Section 4.1)
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POGODINA Maria
The main responsibilities are the ones mentioned on Article 15 of the EU MDR 2017/745:
Compliance with the Vigilance Reporting obligations (Article 87 to 91)
For Investigational devices: Issuance of a signed statement (Annex XV Chapter II Section 4.1)