ABSTRACT

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.

chapter 1|9 pages

Introduction

chapter 2|19 pages

Regulations and Quality Standards

chapter 6|12 pages

Validation Efforts at the Vendor's Site

chapter 7|13 pages

Responsibilities of Vendors and Users

chapter 9|7 pages

Selection and Qualification of a Vendor

chapter 10|13 pages

Installation and Operation

chapter 11|11 pages

Validation of Analytical Methods

chapter 12|11 pages

Maintenance and Ongoing Performance Control

chapter 13|12 pages

Testing of Chromatographic Computer Systems

chapter 15|6 pages

Diagnostics, Error Recording and Reporting

chapter 16|8 pages

Audit/Inspection of Computerized Systems