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  6. [Technical Seminar] Introduction to GMP Seminar

[Technical Seminar] Introduction to GMP Seminar

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last updated:May 15, 2026

日本アイアール
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A clear explanation for those who are planning to get involved in GMP, including those from non-pharmaceutical industries!

This seminar is aimed at those who have recently been assigned to departments related to pharmaceutical GMP or those who are responsible for businesses related to pharmaceutical manufacturing, even if they are not part of a pharmaceutical company. It will explain what the regulations that must be complied with (GMP) require and what their purpose is. The seminar will cover the basic matters of GMP regulations necessary to grasp the overall picture of GMP, including pharmaceuticals, Japan's legal system and GMP, 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.*

    Technical Seminar
20260622_GMPでは説明できないバイオ医薬品の品質判断.png

[Technical Seminar] Introduction to GMP Seminar

20260622_GMPでは説明できないバイオ医薬品の品質判断.png
20260622_GMPでは説明できないバイオ医薬品の品質判断.png
  • Related Link - https://nihon-ir.jp/seminar/gmp-super-introductory…

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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, among others) Date and Time: [In-person attendance][Live streaming] June 8, 2026 (Monday) 10:30 AM - 4:30 PM [Archive streaming] June 10 - June 24 (available for viewing multiple times during the period) 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 Must Pharmaceutical-Related Companies Adhere To? Chapter 7: What Happens If Compliance Is Not Maintained? Chapter 8: Repeated Issues of Fraudulent Manufacturing Chapter 9: What Procedures Are Necessary to Obtain Manufacturing Approval 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.

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