Japan is one of the biggest medical device markets in the world, and almost 50% of products are imported from abroad.
This makes Japan a market with great potential for overseas medical device manufacturers, however the complicated and strict local regulation (PMDact; Pharmaceutical and Medical Device Act) is a barrier for entry and business development.

TÜV SÜD Japan is a registered certification body under the PMDact. We have provided local certification services since 2005 and certified more than 3,700 products.
In this 1-hour webinar with Q&A, our local expert will share basic knowledge about regulation and market access, as well as provide an overview on project handling.


Webinar Details

■ Date:
12 December 2024, Thursday

■Time:
9:00a.m CET

■Duration:
1 hour

■Fee:
Free

■Speaker:
Yuki Yokoyama - TÜV SÜD Japan Ltd.
Yuki Yokoyama has 15 years of experience in PMDact certification services and is responsible for the local certification body business under the PMDact.
He is also a member of the external working group which discusses regulation with the competent authority and industrial groups.

■How to Register:
Please fill out the application form on this page.

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