Microbial Contamination Control in the Pharmaceutical Industry
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agar
Aseptic Processing
ATP Bioluminescence
Bacillus Stearothermophilus
broth
Burkholderia Cepacia
Category=PS
count
digest
Dry Heat
environments
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Gel Clot
High Throughput Screening
Incubation Time
LAL Assay
LAL Test
Low Nutrient Media
LPS Molecule
maltophila
Moisture Content
Nonsterile Pharmaceutical
Nonsterile Products
PCA
Pharmaceutical Environments
plate
product
R2A Agar
SCDB
Soybean Casein Digest
Soybean Casein Digest Agar
soybean-casein
stenotrophomonas
Sterility Assurance
Sterilization Process
Test Article
TSA Medium
Product details
- ISBN 9780367393946
- Weight: 430g
- Dimensions: 152 x 229mm
- Publication Date: 17 Oct 2019
- Publisher: Taylor & Francis Ltd
- Publication City/Country: GB
- Product Form: Paperback
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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.
Luis Jimenez
