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Post Market Surveillance for Medical Devices 2012
26 Sep 2012
Webinar
Home
Post Market Surveillance for Medical Devices 2012
Key Topics
US System
Medical Device Reports
Complaints (QSR)
Corrections and Removals
The Structure of Post Market Surveillance
Post Production Information Collection
Clinical Evaluation (MDD Annex X)
Risk Management (ISO 14971)
International Systems
EU Vigilance
Complaints (ISO 13485)
Canada Adverse Event Reporting
EU FSCA and FSN
Who should Attend
Regulatory Affairs Managers, Quality Managers, Design Control Managers and Risk Managers.
Read more
Past Events
Post Market Surveillance for Medical Devices 2012 - 26 Sep 2012, Webinar
(31910)
Post Market Surveillance for Medical Devices 2026
Important
Please, check "Post Market Surveillance for Medical Devices" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine:
Healthcare, Medical device, Medical technology
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