Guideline for submitting documentation for the manufacture of and controls for drug products.
| Other author | Center for Drugs and Biologics (U.S.) |
| Other author | Center for Drug Evaluation and Research (U.S.) |
| Format | Electronic |
| Publication Info | Rockville, Md. : Center for Drugs and Biologics, Food amd [sic] Drug Administration, U.S. Dept. of Health and Human Services, [1987] |
| Description | 1 electronic resource (17 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS121022 |
| Subjects |
| Variant title | Title from cover page: Guidance for industry |
| General note | "Center for Drug Evaluation and Research"--Cover p. |
| General note | "February 1987." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Issued in other form | Print version: Guideline for submitting documentation for the manufacture of and controls for drug products |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:D 65 |