
Principles of Parenteral Solution Validation
A Practical Lifecycle Approach
- 298 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
Principles of Parenteral Solution Validation
A Practical Lifecycle Approach
About this book
Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using a lifecycle approach, this book discusses the latest technology, compliance developments, and regulatory considerations and trends, from process design, to divesting. As part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin, this book incorporates numerous case studies and real-world examples that address timely problems and offer solutions to the daily challenges facing practitioners in this area.- Discusses international and domestic regulatory considerations in every section- Features callout boxes that contain points-of-interest for each segment of the audience so readers can quickly find their interests and needs- Contains important topics, including risk management, the preparation and execution of properly designed studies, scale-up and technology transfer activities, problem-solving, and more
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Information
Table of contents
- Cover image
- Title page
- Table of Contents
- Copyright
- Dedication
- List of Contributors
- Editor Biographies
- About the Expertise in Pharmaceutical Process Technology Series
- Introduction
- Chapter 1. Process Validation: Design and Planning
- Chapter 2. Aseptic Process Validation: Aseptic Process Simulation Design
- Chapter 3. Quality Risk Management of Parenteral Process Validation, Part 1: Fundamentals
- Chapter 4. Equipment Cleaning Process
- Chapter 5. Quality Risk Management of Parenteral Process Validation, Part 2: A Risk-Based Quality Management System
- Chapter 6. Use of Statistics in Process Validation
- Chapter 7. Process Validation Stage 1: Parenteral Process Design
- Chapter 8. Process Validation Stage 2: Parenteral Process Performance Qualification
- Chapter 9. Process Validation Stage 3: Continued Process Verification
- Chapter 10. Preuse/Poststerilization Integrity Testing of Sterilizing Grade Filter
- Chapter 11. Environmental Monitoring
- Chapter 12. Isolators
- Chapter 13. Post Aseptic Fill Sterilization and Lethal Treatment
- Conclusion
- Index