Medical Device Reporting Requirements for Manufacturers Final Guidance 2017 is a webinar that covers topics such as:
- 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?"
Medical Device Reporting Requirements for Manufacturers Final Guidance 2017 is intended for 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