Biocontamination Control for Pharmaceuticals and Healthcare
Autor Tim Sandleen Limba Engleză Paperback – 16 feb 2024
This book offers professionals in pharma quality control and related areas guidance on building a complete biocontamination strategy.
- Includes the most current regulations
- Contains three new chapters, including Application of Quality Risk Management and its Application in Biocontamination Control, Designing an Environmental Monitoring Programme, and Synthesis: An Anatomy of a Contamination Control Strategy
- Offers practical guidance on building a complete biocontamination strategy
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ELSEVIER SCIENCE – 16 feb 2024 | 812.27 lei 5-7 săpt. | |
ELSEVIER SCIENCE – 4 dec 2018 | 834.36 lei 5-7 săpt. |
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Specificații
ISBN-13: 9780443216008
ISBN-10: 0443216002
Pagini: 508
Dimensiuni: 191 x 235 x 29 mm
Greutate: 1.03 kg
Ediția:2
Editura: ELSEVIER SCIENCE
ISBN-10: 0443216002
Pagini: 508
Dimensiuni: 191 x 235 x 29 mm
Greutate: 1.03 kg
Ediția:2
Editura: ELSEVIER SCIENCE
Cuprins
1. Introduction
2. Sources of biocontamination, other forms of contamination, and risk profiling
3. GMP, regulations and standards
4. Biocontamination control
5. Application of Quality Risk Management and its application in biocontamination control
6. Introduction to cleanrooms and environmental monitoring
7. Viable monitoring methods
8. Selection of culture media
9. Airborne particle monitoring
10. Rapid microbiological methods11. Designing an environmental monitoring programme
11. Putting an environmental monitoring plan together: A risk-based case study
12. Special Types of Environmental Monitoring
13. Cleanrooms and microbiota
14. Assessment of pharmaceutical water systems
15. Data handling and trend analysi
16. Bioburden and endotoxin assessment of pharmaceutical processing
17. Risk assessment and investigation for environmental monitoring: Examples of microbial data deviations
18. Assessing and removing contamination risks from the process
19. The human factor: Training and controlling people in cleanrooms
20. Biocontamination deviation management
21. Synthesis: An anatomy of a contamination control strategy
2. Sources of biocontamination, other forms of contamination, and risk profiling
3. GMP, regulations and standards
4. Biocontamination control
5. Application of Quality Risk Management and its application in biocontamination control
6. Introduction to cleanrooms and environmental monitoring
7. Viable monitoring methods
8. Selection of culture media
9. Airborne particle monitoring
10. Rapid microbiological methods11. Designing an environmental monitoring programme
11. Putting an environmental monitoring plan together: A risk-based case study
12. Special Types of Environmental Monitoring
13. Cleanrooms and microbiota
14. Assessment of pharmaceutical water systems
15. Data handling and trend analysi
16. Bioburden and endotoxin assessment of pharmaceutical processing
17. Risk assessment and investigation for environmental monitoring: Examples of microbial data deviations
18. Assessing and removing contamination risks from the process
19. The human factor: Training and controlling people in cleanrooms
20. Biocontamination deviation management
21. Synthesis: An anatomy of a contamination control strategy