
Microbial Contamination Control in the Pharmaceutical Industry
Luis Jimenez(Editor)
CRC Press
1st Edition
Published on 17. October 2019
Book
Paperback/Softback
328 pages
978-0-367-39394-6 (ISBN)
Description
This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and procedures used to prevent the microbial contamination of pharmaceutical processes, products, and environments. It identifies new tools for sample analysis and evaluation and the impact of these advancements on the continuous supply and manufacturing of pharmaceutical products. With more than 100 tables and 430 current references, the book contains a detailed analysis of microbial contamination recalls for nonsterile and sterile pharmaceutical products, demonstrating the distribution of microorganisms worldwide and the identification by geographical regions.
More details
Language
English
Place of publication
London
United Kingdom
Publishing group
Taylor & Francis Ltd
Target group
Professional and scholarly
Academic and Professional Practice & Development
Dimensions
Height: 229 mm
Width: 152 mm
Thickness: 18 mm
Weight
480 gr
ISBN-13
978-0-367-39394-6 (9780367393946)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

E-Book
11/2004
1st Edition
CRC Press
€89.99
Available for download

Book
08/2004
1st Edition
CRC Press
€262.70
Shipment within 15-20 days

E-Book
08/2004
1st Edition
CRC Press
€89.99
Available for download
Person
Luis Jimenez
Content
Microorganisms in the Environment and Their Relevance to Pharmaceutical Processes; Microbial Limits; Microbial Monitoring of Potable Water and Water for Pharmaceutical Purposes; Sterility Test and Procedures; Environmental Monitoring; Biological Indicator Performance Standards and Control; Rapid Methods for Pharmaceutical Analysis; Endotoxin: Relevance and Control in Parenteral Manufacturing; Proper Use and Validation of Disinfectants; Antimicrobial Effectiveness Test and Preservatives in Pharmaceutical Products