An article authored by Eamonn McGowran, Associate Director of Regulatory Affairs, was recently featured in Med-Tech Innovation – the leading multi-platform communication brand for the UK and Irish medical design and manufacturing industry.
The article. ‘Regulation for medical devices: recent developments explained’ covers the European Commission’s proposal to extend the Medical Device Regulation (MDR) transition period and outlines the key regulatory changes for developers of both devices and medicines to be aware of.
Our Regulatory Affairs team has a wealth of experience in the regulation of medical devices and will be following the developments of the MDR. If you would like to discuss your medical device development, or would like any advice, please get in touch and a member of our team will be happy to help.