Guidance for industry : S7A safety pharmacology studies for human pharmaceuticals.
| 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, [2001] |
| Description | 11 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS113888 |
| Subjects |
| Portion of title | S7A safety pharmacology studies for human pharmaceuticals |
| Portion of title | Safety pharmacology studies for human pharmaceuticals |
| General note | Title from PDF title page (viewed on June 18, 2009). |
| General note | "ICH". |
| General note | "July 2001". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography note | Includes bibliographical references (p. 11). |
| Technical details | Mode of access: Internet at the FDA web site. Address as of 6/18/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm129156.pdf; current access is available via PURL. |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:SA 1/2 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |