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

How to get market access / How to get medical device approval / certification in Japan

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

Programme:

• Introduction
• Expert’s presentation
• Q&A Session

Registration deadline: 19 February 2024

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.

Moderator: Sofia Smerzi, Business Support Coordinator, EU-Japan Centre for Industrial Cooperation

Organiser: EU-Japan Centre for Industrial Cooperation - Brussels Office

Deliverables