EU and US Regulations for Chemical Components in Medical Devices

Posted 31 March 2017 By Kenneth Stanvick

placeholder+image This article discusses a number of regulations directed at the use of chemical components in medical devices, both in the EU and US. The author reviews legislation, offers compliance advice and warns about the penalties of noncompliance.

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Categories: Medical Devices, Compliance, Features, US, Europe, FDA, EC

Tags: Chemical Components, Restricted Substances

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