(MedPage Today) — The FDA has allowed a substantial amount of late reports and undated reports into its Manufacturer and User Facility Device Experience (MAUDE) safety database, researchers confirmed. During a 3.5-year period in 2019-2022, there… Source link : https://www.medpagetoday.com/publichealthpolicy/fdageneral/114622 Author : Publish date : 2025-03-12 22:30:00 Copyright for syndicated content belongs to the linked […]
The post FDA’s Deadline Ignored in Nearly 30% of Device Safety Reports first appeared on News Health.
Author : News Health
Publish date : 2025-03-12 22:30:00
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