After a challenging four years of preparation for the EU IVDR, there is only one year left on the clock. However, after tackling the global COVID-19 pandemic in 2020, is industry ready to meet the IVDR requirements? Do Notified Bodies have the capacity and time to handle all IVDR certificates heading their way? Are PMS and Clinical teams ready to adapt to the longer-term commitments required? And are you confident in the resources you have to maintain compliance once your CE marks are approved?
MedTech Summit is conducting one of the biggest surveys of its kind across our database of medical device and IVD professionals across Europe and the world. The final report will reveal unique insights into the implementation of the EU IVDR, as well as the biggest challenges and how industry insiders are tackling them.
Completing the survey will take just 5 minutes and will give you exclusive early access to the final report. All answers will remain anonymous.
We’re excited to see the results of this unique study and we hope you are too.