Medical Device Post-Market Surveillance Report Services
Comprehensive adverse event report for any device.
The report provides attorneys with a consolidated history of any medical device and includes the following:
- Scope & Background
- Adverse Event Report Details
- Report Type, Source, Reporter Occupation details, etc.
- Keyword Searches for Device Problems (whether coded or not)
- Trends over time and patterns of violations
- Excel Export with link to each report in Public MAUDE
- Applicable FDA and Industry Articles and Publications