[Seminar/Training] Regulations Related to Chinese Medical Devices: Seminar on New China GMP Explanation

テュフズードジャパン東京本社

In November 2025, the revised "Good Manufacturing Practice (GMP) for Medical Devices" in China will be announced, with implementation scheduled for November 2026. Local experts will provide a clear explanation of the key points for compliance. < Seminar Topics > - Overview of China's new GMP - Differences from ISO 13485:2016 - New requirements that require particularly careful measures - Anticipated inspection styles

Date and time Tuesday, Oct 06, 2026
01:30 PM ～ 05:00 PM
Capital
Entry fee Charge 42,000 yen (including text fee, tax included)

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[Seminar/Training] China Medical Devices New China GMP Explanation Seminar
On October 6, local experts will explain the points of the new Chinese GMP compliance to be implemented in November 2026.

Date and Time: October 6, 2026 (Tuesday) 13:30 - 17:00 Venue: Online Seminar Topics: - Overview of China's new GMP - Differences from ISO 13485:2016 - New requirements that require particularly careful measures - Anticipated inspection styles Target Audience: Japanese manufacturers exporting medical devices and IVD products to China Application Method: Please apply through the seminar website.

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[Seminar/Training] Regulations Related to Chinese Medical Devices - Seminar on New China GMP Explanation

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