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Sterile Processing of Pharmaceutical Products : Engineering Practice, Validation, and Compliance in Regulated Environments

By: (Author) Sam A. Hout

Extended Catalogue

Ksh 23,950.00

Format: Hardback or Cased Book

ISBN-10: 1119802326

ISBN-13: 9781119802327

Publisher: John Wiley & Sons Inc

Imprint: John Wiley & Sons Inc

Country of Manufacture: US

Country of Publication: GB

Publication Date: Jan 21st, 2022

Print length: 368 Pages

Weight: 644 grams

Dimensions (height x width x thickness): 16.00 x 23.90 x 2.80 cms

Product Classification: Chemistry

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Describes the methodologies and best practices of the sterile manufacture of drug products Thoroughly trained personnel and carefully designed, operated, and maintained facilities and equipment are vital for the sterile manufacture of medicinal products using aseptic processing. Professionals in pharmaceutical and biopharmaceutical manufacturing facilities must have a clear understanding of current good manufacturing practice (cGMP) and preapproval inspection (PAI) requirements. Sterile Processing of Pharmaceutical Products: Engineering Practice, Validation, and Compliance in Regulated Environments provides up-to-date coverage of aseptic processing techniques and sterilization methods. Written by a recognized expert with more than 20 years of industry experience in aseptic manufacturing, this practical resource illustrates a comprehensive approach to sterile manufacturing engineering that can achieve drug manufacturing objectives and goals. Topics include sanitary piping and equipment, cleaning and manufacturing process validation, computerized automated systems, personal protective equipment (PPE), clean-in-place (CIP) systems, barriers and isolators, and guidelines for statistical procedure. Offering authoritative guidance on the key aspects of sterile manufacturing engineering, this volume: Covers fundamentals of aseptic techniques, quality by design, risk assessment and management, and operational requirementsAddresses various regulations and guidelines instituted by the FDA, ISPE, EMA, MHRA, and ICHProvides techniques for systematic process optimization and good manufacturing practice Emphasizes the importance of attention to detail in process development and validationFeatures real-world examples highlighting different aspects of drug manufacturing Sterile Processing of Pharmaceutical Products: Engineering Practice, Validation, and Compliance in Regulated Environments is an indispensable reference and guide for all chemists, chemical engineers, pharmaceutical professionals and engineers, and other professionals working in pharmaceutical sciences and manufacturing.

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