{"id":13231,"date":"2025-12-01T15:09:00","date_gmt":"2025-12-01T06:09:00","guid":{"rendered":"https:\/\/microncro.com\/?p=13231"},"modified":"2026-06-04T23:33:08","modified_gmt":"2026-06-04T14:33:08","slug":"webinar20251201","status":"publish","type":"post","link":"https:\/\/microncro.com\/en\/archives\/post\/webinar20251201\/","title":{"rendered":"Tigermed-Jyton and Micron Joint Webinar: Regulatory Framework and Key Points for Medical Device Development in Japan"},"content":{"rendered":"\n

Tigermed-Jyton, a China-based company with extensive experience in supporting medical device development, together with Micron, will host a webinar on regulatory requirements for medical devices in Japan. The session will provide an overview of key points to consider when developing and applying for medical device approval in Japan.
*Please note that the webinar will be conducted in Chinese.<\/p>\n\n\n\n

Date and Time: December 11, 2025 (Thursday), 3:00 PM \u2013 4:00 PM JST<\/p>\n\n\n\n

Speaker: Zheng Tong (Micron, Inc.)<\/p>\n\n\n\n

Link to watch the live webinar: https:\/\/live-watch.bioisp.com\/watch\/6888275<\/a>
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Key Topics
\u2013 Overview of medical device regulations in Japan
\u2013 Approval process and associated costs
\u2013 Key points for PMDA consultation<\/p>\n\n\n\n

If the Chinese-language format is suitable for you, we would be pleased to have you participate in the webinar.<\/p>\n\n\n\n

Please contact :
Micron, Inc. Sales promotion Dept.
E-mail\uff1ainfo@micron-kobe.com:<\/strong><\/p>\n\n\n\n\n

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