Validation of Pharmaceutical Processes: 3rd Edition (e-Book) book cover

Validation of Pharmaceutical Processes

3rd Edition

Edited by James P. Agalloco, Frederick J. Carleton

CRC Press

760 pages

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Hardback: 9780849370557
pub: 2007-09-25
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pub: 2007-09-25
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Description

Completely revised and updated to reflect the significant advances in pharmaceutical production and regulatory expectations, this third edition of Validation of Pharmaceutical Processes examines and blueprints every step of the validation process needed to remain compliant and competitive. The many chapters added to the prior compilation examine va

Table of Contents

Validation of Pharmaceutical Processes, 3E. Why Validation. Organizing for Validation. Validation and Facility Design. Validation of Environmental Control Systems Used in Parenteral Facilities. Validation of Critical Utilities. The Validation of Pharmaceutical Water Systems. Calibration and Metrology. Temperature Measurements. Qualification & Change Control. Microbiology of Sterilization Processes. F, D, and z Values. Steam Sterilization in Autoclaves. Validation of Terminal Sterilization. Steam Sterilization-in-Place Technology and Validation. Dry Heat Sterilization and Depyrogenation Validation and Monitoring. Validation of Ethylene Oxide Sterilization Processes. Validation of Chlorine Dioxide Sterilization. Validation of the Radiation Sterilization of Pharmaceuticals. Isolator Decontamination.

Validation of Sterilizing-Grade Filters. Cleaning and Disinfection in the Control of Pharmaceutical Cleanrooms. Process Simulation. Validation of Aseptic Processing for Bulk Pharmaceutical Chemicals. Validation of Manual Aseptic Processes. Monitoring of Non-viable Particles. Monitoring of Viable Particles. Validation of Component Preparation. Validation of Lyophilization. Qualification Concerns for Isolator Systems.

Validation of Solid Dosage Finished Goods. Validation of Validation of Oral / Topical. Liquids & Semi-Solids. Validation of Packaging Operations. Validation of Bulk Chemical Processes. Validation of Recovery and Purification Processes. Validation of Process Chromatography. Cell Culture Process Validation. Cleaning Validation for the Pharmaceutical, Biopharmaceutical, Cosmetic, Nutraceutical, Medical Device and Diagnostic Industries. Validation of Training. Vendor Validations. Validation for Clinical Manufacturing. Validation of New Products. Retrospective Validation

Validation and Six Sigma. Validation and Contract Manufacturing. Process Analytical Technology and Validation. Computerized Systems Validation

Subject Categories

BISAC Subject Codes/Headings:
MED071000
MEDICAL / Pharmacology