Clearly demonstrate appropriate correction and recording methods in case of deficiencies, and acquire skills for "error-free record management" that can be practiced on-site!
We will hold a seminar titled "How to Reduce Recording Errors: GMP Manufacturing Record Keeping and How to Document When There Are Deficiencies." Based on advanced examples of regulatory authorities in Europe and the United States, we will systematically explain the correct way to write GMP manufacturing records, design formats, and review methods. This program is designed for those involved in the creation and verification of manufacturing records in pharmaceutical companies and related businesses. 【Seminar Overview (Partial)】 ■ Date: March 26, 2026 (Thursday) 10:00 AM - 4:00 PM ■ Venue: Online only (Zoom system) ■ Participation Fee (including tax): 49,500 yen per person ■ Course Materials: 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】 ■Key Points for Creating Manufacturing Records ■Considerations for Creating Manufacturing Records Learned from Regulatory Authority Inspections ■Key Points for Reviewing Manufacturing Records, etc. *For more details, please download the PDF or feel free to contact us.
Price information
■Tuition fee (including tax): 49,500 yen per person
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P2
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For more details, please download the PDF or feel free to contact us.
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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.





