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New Medical Device Regulation (MDR) Training

Meditrial EU compliance series

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 devices and companies.

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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.

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New ISO 14155:2019 Key Changes for your Trial

Meditrial EU compliance series

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!

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Clinical Evaluation from A to Z

Meditrial EU compliance series
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.