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Full Description
Biocontamination Control for Pharmaceuticals and Healthcare, Second Edition outlines a biocontamination strategy that tracks bio-burden control and reduction at each transition in classified areas of a facility. The first edition of the book covers many of the aspects of the strategy, but the new official guidance signals that a roadmap is required to fully comply with its requirements. Completely updated with the newest version of the EU-GPM (EN17141), this new edition expands coverage of quality risk management and contains completely new examples to help professionals bridge the gap between regulation and implementation.
This book offers professionals in pharma quality control and related areas guidance on building a complete biocontamination strategy.
Contents
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
