Medical Device Reporting Requirements for Manufacturers Final Guidance 2017
16 May 2017
Webinar
Description
Topics
Reporting requirements
MDR regulation
Written procedures
Manufacturer reporting requirements
Specific issues and situations
Recordkeeping and public disclosure
Report timing
Malfunction reporting
When do you "become aware?"
Who should Attend
Attendees involved or interested in:
Regulatory Affairs
Clinical Affairs
R&D
Quality
Consultants
Complaint and Risk Management Personnel
Contractors/subcontractors
Senior Management
Other interested parties
Past Events
Medical Device Reporting Requirements for Manufacturers Final Guidance 2017 - 16 May 2017, Webinar (67580)
Important
Please, check "Medical Device Reporting Requirements for Manufacturers Final Guidance" official website for possible changes, before making any traveling arrangements
