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

Name: Sterile Processing of Pharmaceutical Products
Author: Sam A. Hout

Auteur: Sam A. Hout

Taal: Engels

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Uitgever: John Wiley & Sons Inc

Auteur: Sam A. Hout

Engels
Hardcover
9781119802327
21 januari 2022
368 pagina's

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Samenvatting

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 requirements
Addresses various regulations and guidelines instituted by the FDA, ISPE, EMA, MHRA, and ICH
Provides techniques for systematic process optimization and good manufacturing practice
Emphasizes the importance of attention to detail in process development and validation
Features 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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Taal: en
Bindwijze: Hardcover
Oorspronkelijke releasedatum: 21 januari 2022
Aantal pagina's: 368

Betrokkenen

Hoofdauteur: Sam A. Hout
Hoofduitgeverij: John Wiley & Sons Inc

Overige kenmerken

Product breedte: 10 mm
Product hoogte: 10 mm
Product lengte: 10 mm
Studieboek: Nee
Verpakking breedte: 160 mm
Verpakking hoogte: 25 mm
Verpakking lengte: 237 mm
Verpakkingsgewicht: 789 g

EAN

EAN: 9781119802327

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Categorieën: Technologie & Bouwkunde

Industriele chemie

Boeken
Beschikbaarheid: Leverbaar
Boek, ebook of luisterboek?: Boek
Taal: Engels
Studieboek of algemeen: Algemene boeken

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