Study Reveals Medical Device Makers Frequently Delay Safety Reports to FDA

A new study published in The BMJ has uncovered significant delays in medical device manufacturers reporting adverse events to the Food and Drug Administration (FDA).  The study analyzed 4.4 million manufacturer reports from 2019 to 2022 and found that nearly 14% (600,000 reports) were submitted late, while another 600,000 had missing or invalid dates. Most […]