Product Key Features
Number of Pages576 Pages
Publication NameGood Design Practices for Gmp Pharmaceutical Facilities
LanguageEnglish
SubjectEnvironmental / General, Pharmacology
Publication Year2005
TypeTextbook
AuthorTerry Jacobs
Subject AreaTechnology & Engineering, Medical
SeriesDrugs and the Pharmaceutical Sciences Ser.
FormatHardcover
Additional Product Features
Intended AudienceScholarly & Professional
LCCN2005-048455
Reviews"immensely informative, rich in detail, and well-indexed.a useful addition to the company library." -Organic Process Research and Development
Dewey Edition22
Series Volume NumberVol. 143
IllustratedYes
Dewey Decimal615/.19
Table Of ContentPharmaceutical Industry Profile. Current Good Manufacturing Practice. Facility Planning. Architecture. Mechanical/HVAC/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. Building Code Compliance. Containment/Isolation. Occupational Health and Safety. Technology Transfer. Environmental. Support Laboratories. Packaging/Warehousing
SynopsisA convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the production and efficacy of a pharmaceutical facility and the products it produces.
LC Classification NumberTH4541