This book provides an introduction to cleanrooms and clean air devices in GMP environments. The book explains what cleanrooms are, the contamination risks, key design features, and the requirements for classifying and operating them. The book includes detail on the 2015 update to the international cleanroom standard ISO 14644 (Parts 1 and 2).
"synopsis" may belong to another edition of this title.
Dr. Sandle has over twenty-five years experience of microbiological research and biopharmaceutical processing. This includes experience of designing, validating and operating a range of microbiological tests including sterility testing, bacterial endotoxin testing, bioburden and microbial enumeration, environmental monitoring, particle counting and water testing. In addition, Dr. Sandle is experienced in pharmaceutical microbiological risk assessment and investigation.
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Seller: GreatBookPrices, Columbia, MD, U.S.A.
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Seller: CitiRetail, Stevenage, United Kingdom
Paperback. Condition: new. Paperback. This book provides an introduction to cleanrooms and clean air devices in GMP environments. The book explains what cleanrooms are, the contamination risks, key design features, and the requirements for classifying and operating them. The book includes detail on the 2015 update to the international cleanroom standard ISO 14644 (Parts 1 and 2). This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Seller Inventory # 9781533160478
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