Guidance for industry : investigating out-of-specification test results (OOS) for pharmaceutical production.
| Other author/creator | Center for Drug Evaluation and Research (U.S.) |
| Format | Electronic and Book |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2006] |
| Description | 1 online resource (14 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS116638 |
| Subject(s) |
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| Portion of title | Investigating out-of-specification test results (OOS) for pharmaceutical production |
| General note | "Pharmaceutical CGMPs." |
| General note | "October 2006." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:OU 8 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |