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

Date2020-11-09

Deadline2020-10-30

VenueOnline event, USA - United States USA - United States

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

Websitehttps://www.complianceonline.com/eu-mdr-...

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

Other CFPs

  1. BSA/AML Contextual Awareness of High Risk Customers
  2. How to Conduct Successful Supplier Audits
  3. 21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures
  4. Data Integrity Compliance for Computer Systems Regulated by FDA
  5. ISO 14971 Medical Device Risk Management Training

Last modified: 2020-10-05 16:33:17