Validation and Qualification in Analytical Laboratories, Second Edition

Validation and Qualification in Analytical Laboratories, Second Edition

Author: Ludwig Huber

Publisher: CRC Press

Published: 2007-07-23

Total Pages: 0

ISBN-13: 9780849382673

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This Second Edition discusses ways to improve pharmaceutical product quality while achieving compliance with global regulatory standards. With comprehensive step-by-step instructions, practical recommendations, standard operating procedures (SOPs), checklists, templates, and graphics for easy incorporation in a laboratory. This title serves as a complete source to the subject, and explains how to develop and implement a validation strategy for routine, non-routine, and standard analytical methods, covering the entire equipment, hardware, and software qualification process. It also provides guidance on qualification of certified standards, in-house reference materials, and people qualification, as well as internal and third party laboratory audits and inspections.


Validation and Qualification in Analytical Laboratories

Validation and Qualification in Analytical Laboratories

Author: Ludwig Huber

Publisher: CRC Press

Published: 1998-10-31

Total Pages: 336

ISBN-13: 9781574910803

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This book explains how to improve product quality while achieving compliance with the world's regulatory standards. A complete guide and reference, it teaches you how to develop and implement a validation strategy for routine, nonroutine, and standard analytical methods encompassing the entire equipment, hardware, and software qualification process. It includes examples and templates to help speed you through the validation process. Chromatographs, spectrophotometers, titrators, methods, reference compounds, and every possible item and category have been addressed. In addition to guidelines on the qualification of standards, certified and in-house reference materials, and employee qualification, it covers internal and third-party lab audits and inspections. Case studies, checklists, flowcharts, templates, and key SOPs support the text. All major regulations and quality standards are covered: US GLP, GMP, GCP, EN45001, ISO 9000 Series, NAMAS, ISO Guide 25, & corresponding interpretation & inspection guides.


Practical Approaches to Method Validation and Essential Instrument Qualification

Practical Approaches to Method Validation and Essential Instrument Qualification

Author: Chung Chow Chan

Publisher: John Wiley & Sons

Published: 2011-03-01

Total Pages: 363

ISBN-13: 1118060318

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Practical approaches to ensure that analytical methods and instruments meet GMP standards and requirements Complementing 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 systems Part 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 labs At 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.


Quality Assurance in Analytical Chemistry

Quality Assurance in Analytical Chemistry

Author: Bernd Wenclawiak

Publisher: Springer Science & Business Media

Published: 2004

Total Pages: 306

ISBN-13: 9783540405788

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This advanced EURACHEM textbook is designed for training, teaching and continuing studies providing an in-depth but easy to understand coverage of Quality Assurance in Chemical Measurement. The CD-ROM accompanying the book contains course materials of 10 experiencedspecialists in the field withmore than 200 overheads (graphics and text) as ready-to-use Powerpoint R documents. The book will serve as an advanced textbook for analytical chemistry students and professionals in industry and service labs and as a reference text and source of course materials for lecturers. TOC:M. Koch: Basic Statistics.-B. Wenclawiak: Glossary (incl. organisations).-B. Wenclawiak: Fit for Purpose.-M. Koch: Quality Manual.-E. Hadjicostas: Validation of Methods.-R. Kraus: ISO 17025-Accreditation.-E. Hadjicostas: ISO 9000-Certification.-M. Valcarcel: Accreditation vs. Certification.-E. Hadjicostas: Good Laboratory Practice.-R. Kraus: Calibration and Detection Limits.- A. Williams: Measurement Uncertainty.-I. Papadakis: Reference Materials.-M. Koch: Control Charts.-M. Koch: Proficiency Testing.- I. Papadakis: Metrology in Chemistry/Traceability.-B. Wenclawiak: QA in Educational Institutions.-E. Hadjicostas: TQM and Cost of Quality.


Analytical Method Validation and Instrument Performance Verification

Analytical Method Validation and Instrument Performance Verification

Author: Chung Chow Chan

Publisher: John Wiley & Sons

Published: 2004-04-23

Total Pages: 320

ISBN-13: 047146371X

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Validation describes the procedures used to analyze pharmaceutical products so that the data generated will comply with the requirements of regulatory bodies of the US, Canada, Europe and Japan. Calibration of Instruments describes the process of fixing, checking or correcting the graduations of instruments so that they comply with those regulatory bodies. This book provides a thorough explanation of both the fundamental and practical aspects of biopharmaceutical and bioanalytical methods validation. It teaches the proper procedures for using the tools and analysis methods in a regulated lab setting. Readers will learn the appropriate procedures for calibration of laboratory instrumentation and validation of analytical methods of analysis. These procedures must be executed properly in all regulated laboratories, including pharmaceutical and biopharmaceutical laboratories, clinical testing laboratories (hospitals, medical offices) and in food and cosmetic testing laboratories.


Quality Assurance and Quality Control in the Analytical Chemical Laboratory

Quality Assurance and Quality Control in the Analytical Chemical Laboratory

Author: Piotr Konieczka

Publisher: CRC Press

Published: 2018-03-26

Total Pages: 320

ISBN-13: 1315294990

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The second edition defines the tools used in QA/QC, especially the application of statistical tools during analytical data treatment. Clearly written and logically organized, it takes a generic approach applicable to any field of analysis. The authors begin with the theory behind quality control systems, then detail validation parameter measurements, the use of statistical tests, counting the margin of error, uncertainty estimation, traceability, reference materials, proficiency tests, and method validation. New chapters cover internal quality control and equivalence method, changes in the regulatory environment are reflected throughout, and many new examples have been added to the second edition.


Handbook of Analytical Validation

Handbook of Analytical Validation

Author: Michael E. Swartz

Publisher: CRC Press

Published: 2012-04-24

Total Pages: 226

ISBN-13: 0824706897

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Written for practitioners in both the drug and biotechnology industries, the Handbook of Analytical Validation carefully compiles current regulatory requirements on the validation of new or modified analytical methods. Shedding light on method validation from a practical standpoint, the handbook: Contains practical, up-to-date guidelines for analytical method validation Summarizes the latest regulatory requirements for all aspects of method validation, even those coming from the USP, but undergoing modifications Covers development, optimization, validation, and transfer of many different types of methods used in the regulatory environment Simplifying the overall process of method development, optimization and validation, the guidelines in the Handbook apply to both small molecules in the conventional pharmaceutical industry, as well as well as the biotech industry.


Validation of Computerized Analytical Systems

Validation of Computerized Analytical Systems

Author: Ludwig Huber

Publisher: CRC Press

Published: 2023-04-28

Total Pages: 268

ISBN-13: 1000948226

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Validation of Computerized Analytical and Networked Systems provides the definitive rationales, logic, and methodology for validation of computerized analytical systems. Whether you are involved with formulation or analytical development laboratories, chemical or microbiological quality control laboratories, LIMS installations, or any aspect of robotic in a healthcare laboratory, this book furnishes complete validation details. International and FDA regulations and requirements are discussed and juxtaposed with numerous practical examples that show you how to cost-effectively and efficiently accomplish validation acceptable to FDA GCP/GLP/GMP, NAMAS, and EN45001 standards. The templates included provide documentation examples and the many checklists found throughout the book assure that all aspects of covered in a logical sequence. The chapters describe and explain such topics as the Product Life Cycle revalidation, change control, documentation requirements, qualifications, testing, data validation and traceability, inspection, SOPs, and many other that help streamline the validation process.


Analytical Method Development and Validation

Analytical Method Development and Validation

Author: Michael E. Swartz

Publisher: CRC Press

Published: 1997-05-16

Total Pages: 100

ISBN-13: 9780824701154

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Describes analytical methods development, optimization and validation, and provides examples of successful methods development and validation in high-performance liquid chromatography (HPLC) areas. The text presents an overview of Food and Drug Administration (FDA)/International Conference on Harmonization (ICH) regulatory guidelines, compliance with validation requirements for regulatory agencies, and methods validation criteria stipulated by the US Pharmacopia, FDA and ICH.