The Global Medical Device Reporting - A Comparison of Worldwide Regulations 2013 is a webinar that covers topics such as:
- Medical Device Vigilance
- Edical Device Reporting
- Serious injury
- Malfunction
- Who Reports
- Incident
- Timing requirements
- Decision Trees – when to report
- Regulatory agencies next steps
- Comparison of format of reports
- Similar products
- Capital equipment
- Social Media
- Maude Database
- Alternative Summary Report (ASR)
- EMDR
- Remedial Action Exemption (RAR)
The Global Medical Device Reporting - A Comparison of Worldwide Regulations 2013 brings together:
- Medical Device Regulatory affairs professionals
- Medical Device Quality professionals involved in post market surveillance activities
- Consultants in the global medical device regulatory space
- Medical Device Quality Managers / Quality Directors / Quality VPs
- Auditors
- Medical Device Quality Engineers / Quality Assurance Professionals