RSS

In Vitro Diagnostic Medical Devices

An introductory guide has been made available by the Medicine and Healthcare products Regulatory Agency (MHRA) so manufacturers are aware of requirements under the new EU regulations for medical devices (MDR) and in vitro diagnostic devices (IVDR). more

30 Aug 2017 15:30 News

The Regulatory Affairs Professionals Society (RAPS) is hosting a dedicated workshop on the new EU regulations for medical devices and in vitro diagnostic devices. more

22 May 2017 14:55 News