Post-Market Surveillance Report

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

CLICK HERE TO VIEW AN EXAMPLE REPORT.