Cleaning Validation Manual : a Comprehensive Guide for the Pharmaceutical and Biotechnology Industries.
Provides technical solutions to assist in fulfilling the training needs of finished pharmaceutical manufacturers. This work is suitable for those involved in the development, manufacturing, auditing, and validation of bio-pharmaceuticals on a pilot scale, leading to scaled-up production.
Saved in:
| Online Access: |
Full text (MCPHS users only) |
|---|---|
| Main Author: | |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Hoboken :
CRC Press,
2010
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| Subjects: | |
| Local Note: | ProQuest Ebook Central |
MARC
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| 245 | 1 | 0 | |a Cleaning Validation Manual : |b a Comprehensive Guide for the Pharmaceutical and Biotechnology Industries. |
| 260 | |a Hoboken : |b CRC Press, |c 2010. | ||
| 300 | |a 1 online resource (610 pages) | ||
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| 505 | 0 | |a Front cover; Contents; List of Figures; List of Tables; About the Book; Preface; Acknowledgments; Authors; Introduction; Disclaimer; CLV-1: How to Establish a Cleaning Validation Program; Body; CLV-2: Introduction; CLV-3: Scope and Approach; CLV-4: Cleaning Validation Team Membersand Responsibilities; CLV-5: Cleaning Validation Philosophy, Strategies, and Methodology; CLV-6: Planning Phase; CLV-7: Execution Phase; CLV-8: Analytical Testing and Reporting Phase; CLV-9: Equipment Description; CLV-10: Facility Description; CLV-11: Utilities Description: DIW, WFI, Steam, and Compressed Air. | |
| 505 | 8 | |a CLV-12: Utilities Monitoring and Microbiological ControlCLV-13: Equipment Cleaning Materials/DetergentDescription; CLV-14: Microbiological Cleaning of Equipment Surface; CLV-15: Solubility of Active Materials in Water; CLV-16: Toxicity of Active Materials; CLV-17: Cleaning Validation Products Grouping Matrix (Tablets, Capsules, and PPS); CLV-18: Product/Equipment Train Matrix (TabCapPPS); CLV-19: Worst-Case Products (Tablets, Cap. | |
| 520 | |a Provides technical solutions to assist in fulfilling the training needs of finished pharmaceutical manufacturers. This work is suitable for those involved in the development, manufacturing, auditing, and validation of bio-pharmaceuticals on a pilot scale, leading to scaled-up production. | ||
| 588 | 0 | |a Print version record. | |
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| 650 | 0 | |a Drug factories |x Equipment and supplies |x Cleaning |v Handbooks, manuals, etc. | |
| 650 | 0 | |a Biotechnology industries |x Equipment and supplies |x Cleaning |v Handbooks, manuals, etc. | |
| 650 | 0 | |a Medical instruments and apparatus |x Sterilization |v Handbooks, manuals, etc. | |
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