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Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceu
US $125.60
ApproximatelyS$ 161.14
Condition:
Good
A book that has been read but is in good condition. Very minimal damage to the cover including scuff marks, but no holes or tears. The dust jacket for hard covers may not be included. Binding has minimal wear. The majority of pages are undamaged with minimal creasing or tearing, minimal pencil underlining of text, no highlighting of text, no writing in margins. No missing pages.
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Located in: Carrollton, Texas, United States
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eBay item number:335839133602
Item specifics
- Condition
- ISBN
- 9781482258905
About this product
Product Identifiers
Publisher
CRC Press LLC
ISBN-10
1482258900
ISBN-13
9781482258905
eBay Product ID (ePID)
3038728871
Product Key Features
Number of Pages
518 Pages
Language
English
Publication Name
Good Design Practices for Gmp Pharmaceutical Facilities
Subject
Pharmacy, Industries / Pharmaceutical & Biotechnology, Pharmacology, Chemistry / General, Quality Control
Publication Year
2016
Type
Textbook
Subject Area
Science, Business & Economics, Medical
Series
Drugs and the Pharmaceutical Sciences Ser.
Format
Hardcover
Dimensions
Item Height
1.2 in
Item Weight
44.9 Oz
Item Length
10.3 in
Item Width
7.2 in
Additional Product Features
Edition Number
2
Intended Audience
College Audience
LCCN
2016-007232
Dewey Edition
23
Illustrated
Yes
Dewey Decimal
615.1900682
Table Of Content
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.
Edition Description
Revised edition,New Edition
Synopsis
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.
LC Classification Number
RS192
Item description from the seller
Seller feedback (38,574)
- t***t (687)- Feedback left by buyer.Past monthVerified purchaseAs described
- u***6 (2735)- Feedback left by buyer.Past monthVerified purchaseBook arrived as described...Thank You👍
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Seller feedback (38,574)
- t***t (687)- Feedback left by buyer.Past monthVerified purchaseAs described
- u***6 (2735)- Feedback left by buyer.Past monthVerified purchaseBook arrived as described...Thank You👍
- e***e (291)- Feedback left by buyer.Past monthVerified purchaseExcellent