A must-see seminar where you can systematically acquire practical knowledge including comparisons of domestic and international regulations, legal requirements, PQS, and Data Integrity!
Our company will hold a seminar titled "The GMP of Investigational Drugs 2026 – Correct Understanding and Appropriate Operation from the Start of Investigational Drug Manufacturing to Delivery to Clinical Trial Sites." We will explain the trends in investigational drug GMP in anticipation of 2026, covering the entire process from exploratory research to manufacturing, quality assurance, storage, distribution, and delivery to clinical trial sites. This is a must-attend seminar where you can systematically acquire practical knowledge, including comparisons of domestic and international regulations, legal requirements, PQS, and Data Integrity. 【Seminar Overview (Partial)】 ■ Date: December 11, 2025 (Thursday) 10:00 AM – 4:30 PM ■ Venue: TH Planning Seminar Room A ■ Nearest Stations: - Toei Asakusa Line / Mita Line: Mita Station, 3-minute walk (A9 exit) - JR Tamachi Station: 7-minute walk (Mita exit) ■ Participation Fee (including tax): 49,500 yen per person ■ Course Materials: Bound textbook + PDF materials (included in the participation fee) *Please apply early as the registration will close once the capacity is reached.
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basic information
【Acquired Knowledge】 ■ GMP, GQP, GDP, GCTP, GCP, PQS, Data Integrity, etc. ■ Pharmaceuticals, pharmaceutical development, clinical trials, approval applications, reliability assurance, quality and quality assurance of pharmaceuticals and investigational drugs ■ Regulations related to pharmaceuticals and investigational drugs (Japan, Europe, USA, PIC/S, WHO) ■ GMP for investigational drugs, GMP for pharmaceuticals, supply chain for pharmaceuticals and investigational drugs (storage, distribution, delivery), etc. *Please apply early as the application will close once the capacity is reached.
Price information
■Tuition fee (including tax): 49,500 yen per person
Price range
P2
Delivery Time
Applications/Examples of results
Please apply as soon as possible, as the application will close once the capacity is reached.
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Download All Catalogs![GMP for Investigational Drugs 2026 - Correct Understanding and Appropriate Operation from the Start of Investigational Drug Manufacturing to Delivery to Clinical Trial Sites - [Seminar Leaflet]](https://image.mono.ipros.com/public/catalog/image/2115080/IPROS8711498381155729650.jpeg?w=120&h=170)
Company information
TH Planning Co., Ltd. is a company that conducts technical seminars, dispatches instructors for training, and provides technical consulting. We aim to contribute to the development of manufacturing and value creation by creating educational opportunities that provide specialized knowledge and know-how in technology and by becoming a hub that connects technologies. Please feel free to contact us when you need our services.
