FY 2026 GMP Case Study Workshop

July 23, 2026
Japan Pharmaceutical Manufacturers Association Quality & Technology Committee
Chairperson: Eiji Okada
Japan Pharmaceutical Information Center (Public Interest Incorporated Foundation)
Chairman: Jiro Akagawa

In recent years, the environment surrounding the pharmaceutical industry has undergone significant changes, and numerous challenges have emerged in both regulatory and operational aspects, including strengthening stable supply systems, preventing the recurrence of quality incidents, ensuring data integrity, and building trust in contract manufacturing.Under these circumstances, marketing authorization holders and manufacturers are required to establish more advanced and effective risk-based quality assurance systems.
Against this backdrop, the JPMA Quality & Technology Committee will hold the “53rd FY2026 GMP Case Study Seminar” as part of its FY2026 business activities, under the theme “Integration of On-Site Capabilities, Equipment Reliability, and Digital Utilization to Enhance the Effectiveness of Quality Assurance,” as outlined below.This case study seminar is open not only to members of the JPMA but also to a wide range of participants from government agencies and the industry. We look forward to your participation.

Date, Time, and Venue

Participation Fee

Please complete the payment process via the “payment screen” provided after you register. Payment is generally made by credit card (bank transfer is also accepted).

How to Register

(1) How to Register

Please visit the JTB website at the URL below and register for the event via the “New Registration” option.

https://convention.jtbcom.co.jp/data/jpma/

Payment of the participation fee is generally made by credit card. Please complete the payment process via the “Payment Screen” provided after you register. Once we confirm your payment, we will send you a separate email with details on how to connect to the webinar and download the materials.

(2) Important Notes and Requests Regarding Registration

When registering, please enter your company name and select either “JPMA Member” or “Non-Member.” Government agency representatives should select “Government Agency.” Pharmaceutical manufacturing and analytical subsidiaries of JPMA members will be treated as members. When registering, please select the parent company name from the drop-down menu.
Please note that manufacturing and analytical subsidiaries must meet all of the following conditions:

(3) Application Deadline

Attachment

Invitation to Participate in the 53rd GMP Case Study Seminar (FY 2026)

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