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Webinar – Regulations about medical devices in EU and Japan

We are pleased to announce to organize the joint educational webinar on Tuesday, September 5th at 16:00(JST).

This joint webinar is co-organized by Eclevar, a CRO specialized in medtech industry headquarted in Paris, France, Micron, a Japanese CRO with special expertise in molecular imaging, and Tohoku University Knowledge Cast, a consultancy specialized in medical device development. 

This webinar is free of charge. Please participate in to learn about important requirements and some key tips for clinical studies related to your medical device products in EU as well as Japan.

We will also be planning to organize a series of webinars in coming months.

Webinar Program:
Date/time: Tuesday, September 5th, 16:00 ~ 17:30 JST


Topic “TBD” by Tohoku University Knowledge Cast (30min. including Q&A)
Speaker: Mr. Tomohito Suzuki (a senior consultant, a former PMDA reviewer)

Topic “Clinical Study for SaMD-Overview of Imaging Support System and Case Studies-” by Micron (30 min. including Q&A)
Speaker: Mr. Hokuto Ono (Imaging Science Department)

Topic “CER required under EU MDR (tentative)” by Eclevar Medtech
Ms. Yukako Oshima (Clinical Project Manager)

How to participate in the webinar:

Please register to the webinar from the webinar link below to join the webinar.
Note: please enter your full name, your company and department, and your work e-mail address. If you provide e-mail address with gmail or hot-mail, etc, we may not accept your registration.

Note: Upon registration, you will be asked to enter your full name and e-mail address once again to confirm your registration