Quality review, regulation, and business viability assessment in the research and development strategy of new modalities.

TECHNICAL INFOMATION INSTITUTE CO.,LTD
■ Instructors 【Part 1】 Arthur D. Little Japan, Inc. Partner Ryo Hanamura Consultant Eiji Yoshida 【Part 2】 Independent Administrative Institution Pharmaceuticals and Medical Devices Agency (PMDA) Specialist (Biological Quality) Yo Sakurai 【Part 3】 Anderson Mori & Tomotsune Foreign Law Joint Enterprise Patent Attorney Yosuke Kawasaka ■ Event Details Date and Time: September 14, 2023 (Thursday) 10:00 AM - 5:15 PM Venue: Live streaming via Zoom *No lectures will be held at the venue Please check "here" for connection confirmation and attendance procedures for the live seminar. Participation Fee: 60,500 yen per person (including tax and materials) [If two or more participants from the same company apply simultaneously, the fee is 55,000 yen per person (including tax)] [Discounts are available for universities, public institutions, and medical institutions. Please see "Academic Pricing" above for details.]

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Date and time Wednesday, Sep 14, 2022
10:00 AM ~ 05:15 PM
- Capital Online: Live streaming using Zoom
- Entry fee Charge