GMP-related work for beginners / new personnel
This seminar is aimed at individuals newly assigned to departments related to pharmaceutical GMP and those responsible for pharmaceutical manufacturing operations. It will explain what regulations (GMP) need to be complied with and what their objectives are. The seminar will cover the basic elements of GMP regulations necessary to grasp the overall picture of GMP, including pharmaceuticals, the Japanese legal system, the origins of GMP, GMP compliance inspections, and the management tasks stipulated by GMP regulations. *For more details, please check the related links or the seminar details in the catalog.*
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<Event Information> Format: In-person attendance / Live streaming (Zoom) / Archive streaming Location: Japan IR Co., Ltd. Headquarters Seminar Room (3 minutes walk from Akihabara Station, etc.) Date and Time: [In-person attendance][Live streaming] November 16, 2026 (Monday) 10:30 AM - 4:30 PM [Archive streaming] November 18 - December 2 (available for viewing multiple times) Participation Fee: 59,400 yen per person (tax included) Instructor: Kazuhiko Arai (Representative of C&J)
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<Seminar Program (Tentative)> Chapter 1: What is a Pharmaceutical? Chapter 2: Japan's Legal System and GMP Chapter 3: What is GMP? Chapter 4: The Origins of GMP Chapter 5: What Does GMP Require? Chapter 6: What Pharmaceutical-Related Companies Must Adhere To Chapter 7: What Happens If Compliance is Not Maintained? Chapter 8: Recurring Issues of Fraudulent Manufacturing Chapter 9: What Procedures Are Necessary to Obtain Manufacturing Licenses for Pharmaceuticals? Chapter 10: GMP Compliance Inspection Chapter 11: Management Duties Specified by GMP Ordinance
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We support Japan's "monozukuri" (manufacturing) with reliable services ranging from patent research and other intellectual property business solutions to technical translation services and intellectual property/engineer education. We offer high-quality services backed by over 40 years of experience at reasonable prices.
