EU and US Regulations for Chemical Components in Medical Devices
By Kenneth Stanvick -
Published 31 March 2017
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.
Categories: Features, Europe, US, EC, FDA, Compliance, Medical Devices
Tags: Chemical Components, Restricted Substances