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Creating Toxicological Risk Assessments for Medical Devices

Eurofins Medical Device Testing

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Eurofins Medical Device Testing
Creating Toxicological Risk Assessments for Medical Devices

Creating Toxicological Risk Assessments for Medical Devices

Whitepaper – Eurofins Medical Device Testing

There has been a substantial increase in the medical device adverse event reports submitted to the Food and Drug Administration (FDA), by 505% from 2012 to 2022. In 2022, nearly 900 medical devices were recalled by FDA, impacting tens of millions of medical devices.