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  6. [Book] Latest GMP and Related ICH Guidelines (No. 2263)

[Book] Latest GMP and Related ICH Guidelines (No. 2263)

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2263 Latest GMP

last updated:Oct 04, 2024

TECHNICAL INFOMATION INSTITUTE CO.,LTD
TECHNICAL INFOMATION INSTITUTE CO.,LTD
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[Available for preview] How to implement changing regulations in your own factory? A practical guide for response.

Book Title: Practical Compliance with the Latest GMP and Related ICH Guidelines --------------------- ★ Thorough and comprehensive explanation of key points of the revised GMP, including data integrity, risk management, PQS, and supply chain management! ★ Requirements and countermeasures for related guidelines such as ICH Q3C, Q3D, M7 (Impurities GL), and Q13 (Continuous Manufacturing GL)! --------------------- ■ Breakdown of GMP requirements in response to changing regulations and ongoing transformations in digital technology! 【1】 Requirements for building a Quality System (PQS) and specific countermeasures 【2】 GMP documentation and its creation and management 【3】 Quality assurance and audits in line with PQS 【4】 Response to Data Integrity (DI) 【5】 Prevention of cross-contamination 【6】 Impurity regulations and required management strategies 【7】 Promotion of digital transformation (DX) in pharmaceutical factories and response to GMP and DI 【8】 Management strategies for continuous manufacturing, GMP compliance, and implementation examples

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2263

[Book] Latest GMP and Related ICH Guidelines (No. 2263)

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■ Table of Contents Chapter 1: Requirements for Building a Quality System (PQS) and Specific Response Methods Chapter 2: GMP Documents and Their Creation and Management in Response to Revised GMP Chapter 3: Quality Assurance and Auditing of Pharmaceuticals in Response to Revised GMP and PQS Chapter 4: Response to Data Integrity (DI) Chapter 5: Prevention of Cross-Contamination Required by Revised GMP and Domestic and International GMP Chapter 6: Regulations on Impurities and Required Management Strategies Chapter 7: Promotion of DX in Pharmaceutical Factories and Response to GMP and DI Chapter 8: Regulatory Response and Management Strategies for Continuous Production and Process Development --------------------- ●Publication Date: September 30, 2024 ●Format: A4, 667 pages ●Authors: 66 individuals ●ISBN: 978-4-86798-041-5 ---------------------

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[Book] Practical Compliance with the Latest GMP and Related ICH Guidelines (No. 2263)

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[Book] Practical Compliance with the Latest GMP and Related ICH Guidelines (No. 2263)

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How to Implement Changing Regulations in Your Own Factory? A Practical Guide for Response ★ Thorough and comprehensive explanation of key points of the revised GMP, including data integrity, risk management, PQS, and supply chain management! ★ Requirements and countermeasures related to ICH Q3C, Q3D, M7, Q13, and other relevant GLs! --------------------- ■ Table of Contents Chapter 1: Requirements and Specific Response Methods for Building a Quality System (PQS) Chapter 2: GMP Documents and Their Creation and Management in Response to Revised GMP Chapter 3: Quality Assurance and Auditing of Pharmaceuticals in Response to Revised GMP and PQS Chapter 4: Response to Data Integrity (DI) Chapter 5: Prevention of Cross-Contamination Required by Revised GMP and Domestic/International GMP Chapter 6: Regulations on Impurities and Required Management Strategies Chapter 7: Promotion of DX in Pharmaceutical Factories and Response to GMP and DI Chapter 8: Regulatory Response and Management Strategies for Continuous Production and Process Development --------------------- ● Publication Date: September 30, 2024 ● Format: A4, 667 pages ● Authors: 66 ● ISBN: 978-4-86798-041-5 ---------------------

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