Good design practices for GMP pharmaceutical facilities / edited by Terry Jacobs, Andrew A. Signore.
Series: Drugs and the pharmaceutical sciences ; v. 214.Publisher: Boca Raton : CRC Press/Taylor & Francis Group, 2017Copyright date: ©2017Edition: Second editionDescription: xviii, 516 pages : illustrations ; 24 cmContent type:- text
- unmediated
- volume
- 9781482258905 (alk. paper)
| Item type | Current library | Home library | Collection | Call number | Materials specified | Copy number | Status | Date due | Barcode | |
|---|---|---|---|---|---|---|---|---|---|---|
| AM | PERPUSTAKAAN DR ABDUL LATIFF | PERPUSTAKAAN DR ABDUL LATIFF KOLEKSI AM-P. DR ABDUL LATIFF | - | QV778.G646 2017 9 (Browse shelf(Opens below)) | 1 | Available | 00002199189 |
Preceded by: Good design practices for GMP pharmaceutical facilities / Andrew A. Signore, Terry Jacobs. Boca Raton : Taylor & Francis, 2005.
Includes bibliographical references and index.
Pharmaceutical industry profile -- Current good manufacturing practices -- Legacy facility master planning -- Architectural design issues -- Facility utility systems -- High purity water -- Commissioning, qualification, and validation -- Process engineering -- Oral solid dosage facilities -- Continuous oral solid dose processing -- Sterile manufacturing facilities -- Biotechnology facilities -- Codes and standards -- Containment technology -- Occupational health and safety -- Sustainability -- QA/QC laboratories and related support spaces -- Packaging and warehousing.
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