Medical Devices

China’s revised medical device GMP takes effect, strengthening quality and contract manufacturing requirements

China’s National Medical Products Administration (NMPA) put its revised Good Manufacturing Practice (GMP) for Medical Devices into effect on 1 November 2026. Issued under...

UK government confirms indefinite recognition of CE-marked medical devices

The UK Government has confirmed that Great Britain intends to recognise CE-marked medical devices and in vitro diagnostic devices (IVDs) certified under the EU...
spot_imgspot_img