Pharmaceutical products are subject to microbiological contamination that can represent a health hazard to the consumer and cause product spoilage, aesthetic changes, and possible loss of drug efficacy.
An edition of Microbial limit and bioburden tests
(1997)
Microbial limit and bioburden tests
validation approaches and global requirements
by Lucia Clontz
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Includes bibliographical references (p. 211-214) and index.
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- Created April 1, 2008
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| September 17, 2021 | Edited by ImportBot | import existing book |
| November 26, 2020 | Edited by MARC Bot | import existing book |
| April 27, 2011 | Edited by OCLC Bot | Added OCLC numbers. |
| July 30, 2010 | Edited by IdentifierBot | added LibraryThing ID |
| April 1, 2008 | Created by an anonymous user | Imported from Scriblio MARC record |