In Vitro Diagnostic Device Regulation (IVDR)

In vitro Diagnostic help and guidance

LRQA has produced a variety of useful resources about the progress and requirements of the new In vitro Diagnostic regulation.

Medical Devices Regulation (MDR)

Medical Device Directive help and guidance

LRQA has produced a variety of useful resources about the progress and requirements of the new medical device regulation.

Oceanz ISO 13485 certification

ISO 13485 help and guidance

LRQA has produced a variety of useful resources about the progress and requirements of ISO 13485.

medical devices transition club

Medical Devices Transition Support Club

LRQA has launched a transition support club for Medical Device and In-Vitro Diagnostic Medical Device manufacturers. By becoming a member you will receive relevant information and support on the new regulations.