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2020 - Supplier Management with the new Medical Device Regulation EU MDR 745/2017



VenueOnline Event, USA - United States USA - United States

KeywordsEU MDR 745/2017; Regulation (eu) 2017/745; Eu mdr checklist


Topics/Call fo Papers

Closer regulatory binding of the ISO to the new EU MDR
Responsibilities for outsourced processes
What are outsourced processes?
Adjustments in the management review
Adjustments in the audit process
How to onboard the supplier?
Examples from outsourced R&D-, manufacturing-, lab-test - processes
Examples from outsourced sales processes

Last modified: 2019-11-08 22:57:15