'About Japan' webinar series 226: Japanese medical device market – Access to the Japanese market and basic regulatory information

Japanese medical device market information, Basic regulatory information, Challenges for market access to Japan, Case study – pitfalls, frequent findings.

In 40 minutes from your desk, discover:

• Japanese medical device market information
• Basic regulatory knowledge

Speaker

Yuki Yokoyama / PAL certification group manager / TÜV SÜD Japan Ltd. ). Expertise: Regulatory affairs under PMDact (Japanese regulation). More than 15 years working experience in medical device certification service under PMD act. Participating in PMD act regulatory working group as representative of organizer from certification bodies.

Registration

Deadline: 19 February 2024

Please find more information via https://www.eu-japan.eu/eubusinessinjapan/library/event/about-japan-webinar-series-227-japanese-medical-device-market.