Guidance for industry : submission of documentation in applications for parametric release of human and veterinary drug products terminally sterilized by moist heat processes.
| Other author | Center for Drug Evaluation and Research (U.S.) |
| Other author | Center for Veterinary Medicine (U.S.) |
| Other author | Center for Biologics Evaluation and Research (U.S.) |
| Format | Electronic |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2010] |
| Description | 1 electronic resource (7 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS120594 |
| Subjects |
| Portion of title | Submission of documentation in applications for parametric release of human and veterinary drug products terminally sterilized by moist heat processes |
| General note | "Center for Drug Evaluation and Research (CDER)." |
| General note | "Center for Biologics Evaluation and Research (CBER)." |
| General note | "CMC." |
| General note | "February 2010." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography note | Includes bibliographical references (p. 7). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:P 21 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |