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2020 - How to Create A PMS Plan and Report According to EU MDR 2017/745 Article 83-86?
Date2020-07-15
Deadline2020-07-05
VenueOnline event, USA - United States 
KeywordsEu mdr 745/2017; Medical device regulation; Iso 13485:2016
Topics/Call fo Papers
How to define a “Post-Market-Surveillance-Process”?
How to create the new required reports for the Notified Body and the Competent Authorities?
How to do adjustments in the management review
How is the Post-Market-Surveillance-Process” connected to clinical evaluation, customer feedback, complaints and vigilance?
How to create the new required reports for the Notified Body and the Competent Authorities?
How to do adjustments in the management review
How is the Post-Market-Surveillance-Process” connected to clinical evaluation, customer feedback, complaints and vigilance?
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Last modified: 2020-06-24 22:58:33