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Post-market surveillance is an essential aspect of maintaining patient safety. However, recent reports have unveiled serious concerns with reporting of medical device failures. Medical Device Developments editor Emma
The post Why the FDA needs to be more transparent when it comes to reporting medical device failures appeared first on NS Medical Devices.NEXT ARTICLE
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The role of medical devices in healthcare is essential. The diversity and innovativeness of this sector contribute significantly to enhance the quality and efficacy of healthcare. Covering a wide range of products, from simple bandages to the...