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(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…
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Source link : https://www.medpagetoday.com/publichealthpolicy/fdageneral/114622
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Publish date : 2025-03-12 22:30:00
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FDA’s Deadline Ignored in Nearly 30% of Device Safety Reports
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