- Import/ Export
- Registration
- Clinical Trials
- Data Management
- Medical Writing
- Financial Support
- Moral Support
- Emotional Support
- Reimbursement Assistance
- Collection, investigation, and assessment of medical device
- Incidents
- Submission of medical device incidents to Competent Authorities
- Expedited Reporting to Authorities
- Follow up and/or final report management
- Training
- Field safety corrective action generation and submission
- Creation and distribution of Field Notices (FSNs)
- Preparation of Periodic Summary Reporting
- Liaison with authorities
- Writing and/or reviewing Standard Operating Procedures
- Audits/inspections and training on Medical Device Vigilance
- Trend Reports to National Competent
- Working as Responsible person
- Storage and protection of medical device incidents records
- Literature search
- Contact point with the Notified Body about
