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2020 - Post Market Surveillance with the new Medical Device Regulation EU MDR 745/2017
Date2020-12-14
Deadline2020-12-04
VenueOnline event, USA - United States 
KeywordsEU MDR 745/2017; Quality management system; Post Market Surveillance
Topics/Call fo Papers
Responsibilities for “Post Market Surveillance” - activities
What reports are required?
What is the input for the reports?
How to create the reports?
How often the reports required?
Adjustments in the management review
How to work with the output of the reports in the quality management system processes and the technical documentation?
What reports are required?
What is the input for the reports?
How to create the reports?
How often the reports required?
Adjustments in the management review
How to work with the output of the reports in the quality management system processes and the technical documentation?
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Last modified: 2020-11-29 21:30:30