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
2nd ed.
by Lucia Clontz
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Rev. ed. of: Microbial limit and bioburden tests for the pharmaceutical industry.
Includes bibliographical references and index.
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- Created November 3, 2008
- 9 revisions
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| December 20, 2020 | Edited by MARC Bot | import existing book |
| October 9, 2020 | Edited by ImportBot | import existing book |
| August 1, 2020 | Edited by ImportBot | import existing book |
| August 18, 2010 | Edited by IdentifierBot | added LibraryThing ID |
| November 3, 2008 | Created by ImportBot | Imported from Library of Congress MARC record |