Good Design Practices for GMP Pharmaceutical Facilities: Drugs and the Pharmaceutical Sciences
Editat de Terry Jacobs, Andrew A. Signoreen Limba Engleză Hardback – 27 iun 2016
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Specificații
ISBN-13: 9781482258905
ISBN-10: 1482258900
Pagini: 534
Ilustrații: 212
Dimensiuni: 178 x 254 x 32 mm
Greutate: 1.28 kg
Ediția:Revised
Editura: CRC Press
Colecția CRC Press
Seria Drugs and the Pharmaceutical Sciences
Locul publicării:Boca Raton, United States
ISBN-10: 1482258900
Pagini: 534
Ilustrații: 212
Dimensiuni: 178 x 254 x 32 mm
Greutate: 1.28 kg
Ediția:Revised
Editura: CRC Press
Colecția CRC Press
Seria Drugs and the Pharmaceutical Sciences
Locul publicării:Boca Raton, United States
Public țintă
Academic and Professional Practice & DevelopmentCuprins
Pharmaceutical Industry Profile. Current Good Manufacturing Practices. Master Planning Legacy Facilities. Architecture. Mechanical Utilities. High Purity Water. Automation and Process Controls. Validation and Facility Design. Process Engineering. Oral Solid Dosage Facilities. Sterile Manufacturing Facilities. Biotechnology Facilities. API Facilities. Compliance Codes and Standards. Containment / Isolation. Occupational Health and Safety. Technology Transfer. Sustainability and LEED for Manufacturing Facilities. Support Laboratories. Packaging / Warehousing.
Notă biografică
Terry Jacobs, Andrew A. Signore
Descriere
This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.