EU Commission Urges Medical Device Manufacturers to Participate in Public Consultation

Date

January 30, 2025

Category

EU Regulations

Description

The European Commission has launched a public consultation on the EU's legislation concerning medical devices and in vitro diagnostic medical devices. This evaluation focuses on the effectiveness, costs, and administrative burdens of the regulations, particularly for small and medium-sized enterprises.

Medical device manufacturers are urged to participate in the consultation, open until March 21, 2025. Feedback can be provided through a 12-week questionnaire available in all 24 EU languages. NSF is actively involved in this initiative and has already supported many manufacturers and their suppliers in successfully implementing the MDR and IVDR.

Take this opportunity to share your views and help shape the future of medical device regulation in Europe!