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Regulatory Affairs, Medical Devices

MedTech 2020 Survey: EU MDR and IVDR Compliance

Posted by on 20 January 2020
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As we enter 2020 with less guidance documents and certified Notified Bodies than expected, the preparation for the MDR is more crucial than ever. With only a few more months on the clock, is industry ready? Can Companies be truly prepared with so much still to be decided with the MDR? Do Notified Bodies have the capacity and time to handle all MDD and MDR certificates heading their way? Meanwhile, we are half way through the IVDR implementation period. What can be learnt from the MDR? What would you do differently and how can IVD companies learn from MDR implementation procedures?

MedTech Summit is conducting one of the biggest surveys of its kind across our database of medical device and IVD professionals around the world. The final report will reveal unique insights into the readiness of industry today as we head towards the key 2020 and 2022 deadlines, as well as the biggest challenges and how industry insiders are tackling them.

Click here to take part in the survey.

Win a 2-day conference pass…

Completing the survey will take just 5 minutes and will give you exclusive early access to the final report. All answers will remain anonymous. Plus, everyone who completes the survey by Sunday 9th February 2020 will be entered into a prize draw for a free 2-day conference pass to MedTech Summit in Dublin on 22 - 26 June 2020 (terms and conditions can be found here).

We’re excited to see the results of this unique study and we hope you are too.

Click here to take part in the survey.

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