2019 - Supplier Management with the new Medical Device Regulation EU MDR 745/2017
Date2019-08-20
Deadline2019-08-20
VenueOnline Event, USA - United States
KeywordsEU MDR 745/2017; Regulation (eu) 2017/745; Regulation 2017/745
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
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
Other CFPs
- Process Validation - Overview of Why and How
- 2020 2nd International Symposium on Computing, Networking and Communications(ISCNC 2020)
- 2020 2nd International Conference on Big Data, IoT, and Cloud Computing (ICBICC 2020)
- Risk-based Design Control - The New Paradigm for Medical Device Design
- 2020 2nd International Conference on Frontiers of Artificial Intelligence and Machine Learning (FAIML 2020)
Last modified: 2019-08-08 23:24:22