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Why the FDA needs to be more transparent when it comes to reporting medical device failures

11:04 EST 14 Feb 2020 | Compelo Medical Devices

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.

Original Article: Why the FDA needs to be more transparent when it comes to reporting medical device failures

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