Evaluation of reporting trends in the MAUDE Database: 1991 to 2022

Adverse event reporting for medical devices is critical for risk mitigation. The Food and Drug Administration's (FDA) Manufacturer and User Facility Device Experience (MAUDE) database serves as a key tool for post-market surveillance, receiving reports from various sources. Ensuring information...

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Bibliographic Details
Main Authors: Meital Mishali, Nadav Sheffer, Oren Mishali, Maya Negev
Format: Article
Language:English
Published: SAGE Publishing 2025-01-01
Series:Digital Health
Online Access:https://doi.org/10.1177/20552076251314094
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