How to Validate a Pharmaceutical Process
Part of the Expertise in Pharmaceutical Process Technology Series
Series: Expertise in Pharmaceutical Process Technology;
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Product details:
- Publisher Elsevier Science
- Date of Publication 17 June 2016
- ISBN 9780128041482
- Binding Paperback
- No. of pages218 pages
- Size 228x152 mm
- Weight 360 g
- Language English 0
Categories
Long description:
"
How to Validate a Pharmaceutical Process provides a ""how toï¿1⁄2 approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a pharmaceutical process. Understanding the ""whyï¿1⁄2 is critical to a successful and defensible process validation, making this book an essential research companion for all practitioners engaged in pharmaceutical process validation.
" MoreTable of Contents:
1. Introduction
Section I What is Process Validation and Why do Process Validation?2. Defining Process Validation3. Brief Review of the Regulations and Guidelines4. The Role of Change Control
Section II Stage I - Process Development5. Starting the Process Validation Program6. Equipment and Utility Qualification7. Dealing with Computers and Automation Validation8. Process Development
Section II Process Qualification 9. The Process Validation Protocol 10. Dealing with Deviations
Section III Continued Process Verification 11. Collecting and Evaluating Production12. Use of Statistical Process Control - pPk, Pk, cPk, cP
Section IV Other Related Activities13. Cleaning- Verification to Validation14. Facility Qualification
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