Guidance for industry : Q1C stability testing for new dosage forms.
| Other author | Center for Drug Evaluation and Research (U.S.) |
| Other author | Center for Biologics Evaluation and Research (U.S.) |
| Other author | International Conference on Harmonisation. |
| Format | Electronic |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [1996] |
| Description | 1 online resource (1 page) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS117628 |
| Subjects |
| Portion of title | Q1C stability testing for new dosage forms |
| General note | "ICH." |
| General note | "November 1996." |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:ST 1/3 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |