Practical Approaches to Method Validation and Essential Instrument Qualification

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Format: eBook
Pub. Date: 2010-08-01
Publisher(s): Wiley
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Summary

Practical approaches to ensure that analytical methods and instruments meet GMP standards and requirementsComplementing the authors' first book, Analytical Method Validation and Instrument Performance Verification, this new volume provides coverage of more advanced topics, focusing on additional and supplemental methods, instruments, and electronic systems that are used in pharmaceutical, biopharmaceutical, and clinical testing. Readers will gain new and valuable insights that enable them to avoid common pitfalls in order to seamlessly conduct analytical method validation as well as instrument operation qualification and performance verification.Part 1, Method Validation, begins with an overview of the book's risk-based approach to phase appropriate validation and instrument qualification; it then focuses on the strategies and requirements for early phase drug development, including validation of specific techniques and functions such as process analytical technology, cleaning validation, and validation of laboratory information management systemsPart 2, Instrument Performance Verification, explores the underlying principles and techniques for verifying instrument performance-coverage includes analytical instruments that are increasingly important to the pharmaceutical industry, such as NIR spectrometers and particle size analyzers-and offers readers a variety of alternative approaches for the successful verification of instrument performance based on the needs of their labsAt the end of each chapter, the authors examine important practical problems and share their solutions. All the methods covered in this book follow Good Analytical Practices (GAP) to ensure that reliable data are generated in compliance with current Good Manufacturing Practices (cGMP).Analysts, scientists, engineers, technologists, and technical managers should turn to this book to ensure that analytical methods and instruments are accurate and meet GMP standards and requirements.

Table of Contents

Overview of Risk Based Approach to Phase Appropriate Validation and Instrument Qualification
Phase Appropriate Method Validation
Analytical Method Verification, Method Revalidation, and Method Transfer
Validation of PAT Applications
The Validation of Near Infrared Systems for Raw Material Identification
Cleaning Validation
Risk Based Validation of laboratory Information Management Systems (LIMS)
Performance Qualification and Verification of Balance
Performance Verification of NIR Spectrophotometers
Operational Qualification in Practice for Gas Chromatography Instruments
Performance Verification on RI, Fluorescence, Evaporative Light Scattering Detection
Instrument Qualification and Performance Verification for Particle Size Instruments
Method Validation, Qualification, and Performance Verification for Total Organic Carbon (TOC) Analyzers
Instrument Performance Verification - Micro Pipettes
Instrument Qualification and Performance Verification for Automated Liquid Handling Systems
Performance Qualification and Verification in Powder X-ray Diffraction
Table of Contents provided by Publisher. All Rights Reserved.

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