Good Design Practices for GMP Pharmaceutical Facilities

Terry Jacobs, Andrew A. Signore (Herausgeber)

Buch | Hardcover

534 Seiten

2016 | 2nd edition
Crc Press Inc (Verlag)
978-1-4822-5890-5 (ISBN)

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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.

Terry Jacobs, Andrew A. Signore

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.

Erscheinungsdatum	15.07.2017
Reihe/Serie	Drugs and the Pharmaceutical Sciences
Zusatzinfo	55 Tables, black and white; 212 Illustrations, color
Verlagsort	Bosa Roca
Sprache	englisch
Maße	178 x 254 mm
Gewicht	1280 g
Themenwelt	Medizin / Pharmazie ► Pharmazie
Themenwelt	Technik
ISBN-10	1-4822-5890-0 / 1482258900
ISBN-13	978-1-4822-5890-5 / 9781482258905
Zustand	Neuware