Destin A. LeBlanc
Cleaning Validation: Practical Compliance Approaches for Pharmaceutical Manufacturing
Cleaning Validation: Practical Compliance Approaches for Pharmaceutical Manufacturing
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Excellent- More about Cleaning Validation: Practical Compliance Approaches for Pharmaceutical Manufacturing
The author emphasizes the importance of timely cleaning validation in the pharmaceutical industry, particularly for upper management, to meet the challenges of science-based and risk-based approaches. The book covers a diverse range of topics, including EMA vs. ISPE cleaning limits, revised Risk-MaPP for highly hazardous products, and protocol limits for yeasts and molds.
Format: Hardback
Length: 204 pages
Publication date: 23 December 2022
Publisher: Taylor & Francis Ltd
The pharmaceutical industry is a dynamic field, constantly evolving in terms of health-based limits. In this context, timely coverage of cleaning validation is crucial. The author encourages pharmaceutical manufacturers, particularly upper management, to embrace the challenges posed by science-based and risk-based approaches to cleaning validation. Drawing on their extensive experience in the field of cleaning validation and hazardous materials, the author delves into various topics, including EMA vs. ISPE on cleaning limits and the revised Risk-MaPP for highly hazardous products in shared facilities. The book covers a wide range of subjects, from protocol limits for yeasts and molds to cleaning validation for homeopathic drug products. By providing comprehensive insights and practical guidance, this book serves as a valuable resource for professionals involved in the pharmaceutical industry.
The pharmaceutical industry is a dynamic field, constantly evolving in terms of health-based limits.
In this context, timely coverage of cleaning validation is crucial.
The author encourages pharmaceutical manufacturers, particularly upper management, to embrace the challenges posed by science-based and risk-based approaches to cleaning validation.
Drawing on their extensive experience in the field of cleaning validation and hazardous materials, the author delves into various topics, including EMA vs. ISPE on cleaning limits and the revised Risk-MaPP for highly hazardous products in shared facilities.
The book covers a wide range of subjects, from protocol limits for yeasts and molds to cleaning validation for homeopathic drug products.
By providing comprehensive insights and practical guidance, this book serves as a valuable resource for professionals involved in the pharmaceutical industry.
Weight: 557g
Dimension: 229 x 152 (mm)
ISBN-13: 9781032430836
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