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Validation of Pharmaceutical Processes: Sterile Products |
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From Book News, Inc.
Revised and expanded from the 1986 . Provides a detailed, single-source reference for designing, qualifying, calibrating, certifying, and validating systems required to prepare aseptic and non-aseptic pharmaceutical products. Compiles compliance and regulatory principles, documentation practices, scientific approaches, and engineering concepts that can be used independently or in combination to validate products,... >> |
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Metrics and Models in Software Quality Engineering (2nd Edition) |
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From Book News, Inc.
Teaches techniques for measuring and improving the quality of the software development process from high-level to low-level design and all phases of reliability. Covers software metrics, reliability models, and models and analysis of program complexity, and discusses in-process metrics, defect removal, and customer satisfaction. Includes case examples from major computer companies and the NASA Software Engineering laboratory. Annotation copyright Book News, Inc.... >> |
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Analytical Chemistry in a GMP Environment: A Practical Guide |
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From Book News, Inc.
Based on the Laboratory Analyst Training and Certification Program, a two-week course developed and implemented by the Johnson and Johnson company, chemists from a range of pharmaceutical companies and a few academic laboratories explain how to comply with the US Food and Drug Administration's Good Manufacturing Practice rules as analytical technologies are changing rapidly. The material is at a level suitable for readers who hold bachelors degrees in chemistry... >> |
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Quality Control
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