Guidance for industry : formal dispute resolution : scientific and technical issues related to pharmaceutical CGMP.
| Format | Electronic |
| 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 (12 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS116706 |
| Subjects |
| Other author/creator | Center for Drug Evaluation and Research (U.S.) |
| Other author/creator | Center for Biologics Evaluation and Research (U.S.) |
| Other author/creator | Center for Veterinary Medicine (U.S.) |
| Other author/creator | United States. Food and Drug Administration. Office of Regulatory Affairs. |
| Portion of title | Formal dispute resolution |
| Portion of title | Scientific and technical issues related to pharmaceutical CGMP |
| General note | "Center for Biologics Evaluation and Research (CBER)." |
| General note | "Center for Veterinary Medicine (CVM)." |
| General note | "Office of Regulatory Affairs (ORA)." |
| General note | "January 2006." |
| General note | "Expiration date: 05/31/2008." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:D 63 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |