European medical technology industry calls for the EU to join the Medical Device Single Audit Program as a Full Member

MedTech Europe and COCIR have published a joint reflection paper calling on the European Union to join the Medical Device Single Audit Program (MDSAP) as a full member, and to enable the recognition of MDSAP certificates for the purpose of CE marking medical devices and In vitro medical devices.

The MDSAP programme has been operational since 2017 and has since proven to increase regulatory efficiency and cooperation. The EU’s full membership would bring multiple benefits and opportunities to a wide array of stakeholders involved in the device certification process, ultimately contributing to faster patient access to innovative medical technologies.

Read the full joint reflection paper below.