FDA’s Deadline Ignored in Nearly 30% of Device Safety Reports
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 2src19-2src22, there…
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 2src19-2src22, there…
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