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Access Meditrial Academy to learn quickly and easily the details of the new Medical Device Regulation (MDR) 745/2017. Everything you need to know about the MDR and how to apply it to a device and company.

Explore Meditrial Academy to learn how to run clinical trials under the new Medical Device Regulation (MDR) 745/2017.  Get ready for the evolutions that will enhance your trials and increase your success. 


Revisions to the ISO 14155 standard covering pre- and post-market clinical investigations for medical devices are expected  in 2019. The updated standard contains key changes that impact the clinical trial design and conduct, risk management, data capture and safety assessments.

Explore these changes to get ready!


Clinical Evaluation from A to Z

New Clinical Evaluation for Medical Devices
Clinical evaluation is essential to obtain the CE mark for a medical device, but also for designing a clinical trial and for the lmarket evaluation of the device's safety and performance. This tutorial provide the A to Z about this procedure.