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Validation

Purchase pharmaceutical validation books, guides, manuals, handbooks and reports from IndustryMatter.com.  Pharmaceutical quality assurance managers, biopharmaceutical quality assurance managers, pharmaceutical manufacturing managers, pharmaceutical manufacturing operations professionals, pharmaceutical engineering personnel, manufacturing technicians, and pharmaceutical production managers purchase reference books, reference guides and reference manuals to stay current with emerging pharmaceutical manufacturing validation trends.

The pharmaceutical validation books and reference guides available assist quality assurance managers to establish documented evidence that provides a high degree of assurance that a specific pharmaceutical manufacturing process will consistently produce a product meeting its pre-determined specifications and quality attributes. Validation in the pharmaceutical industry can be defined as the documented act of demonstrating that a procedure, process, and activity will consistently lead to the expected results. It often includes the qualification of various types of equipment and systems. It is a requirement for Good Manufacturing Practices and other regulatory requirements.  Because many procedures, processes, and activities must be validated, the field of validation in the pharmaceutical industry is usually segmented into a number of subsections which include the following:

  • Cleaning Validation
  • Process Validation
  • Analytical Method Validation
  • Computer System Validation
Many of the most popular pharmaceutical validation, equipment and instrumentation validation, pharmaceutical analytical methods validation, FDA Corrective and Preventive Action (CAPA) compliance, pharmaceutical manufacturing change control implementation and laboratory practice books and guides are listed below.