1 in 3 FDA safety reports filed late or with missing, invalid dates
A new study analyzing the FDA's Manufacturer and User Facility Device Experience database found that nearly one-third of medical device safety reports were not submitted within the 30-day timeframe or had "missing or invalid date data," according to the report.
A new study analyzing the FDA's Manufacturer and User Facility Device Experience database found that nearly one-third of medical device safety reports were not submitted within the 30-day timeframe or had "missing or invalid date data," according to the report.
