19/20 November 2024
The results of a survey conducted by 39 Notified Bodies were published by the EU Commission at the end of 2023. It concerns certifications and applications under the Medical Device/IVD Regulations (MDR/IVDR). What are the results?
The study, which was launched on 2 December 2022 and will run until 1 December 2025, provides an overview of the availability of medical devices and in-vitro diagnostics. The document is very extensive and comprises 39 slides. The data comes from notified bodies recognized under the MDR/IVDR. The data is from July 2023 and was collected from 39 Notified Bodies. Whereby 29 of the notified bodies are accredited under the MDR, 9 under MDR and IVDR and one under IVDR. The data was prepared in great detail. For example, applications and certificates are presented in graphical form according to the various annexes in comparison to fixed points in time. Data regarding combination products ("devices incoporating a medicinal substance") are also listed, for example.
The reasons for rejection of an MDR application are interesting. 75% of applications are rejected because:
The timeframes for obtaining a new certificate are also interesting (quality management system (QMS) vs. quality management system and product):
Issuing certificates took longer when it came to the quality management system and product:
It usually takes 1-3 months from the application to the signing of a written contract between customers and Notified Bodies (based on feedback from 34 Notified Bodies). More detailed information on in-vitro diagnostics is then available.
The comprehensive results of the survey can be consulted on the EU website.
In January 2024, the EU Commission also published an overview ("dashboard") of the results regarding the availability of medical devices and IVDs in the EU on its website.