Guidance for industry : presenting risk information in prescription drug and medical device promotion.
| Format | Electronic |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research, [2009] |
| Description | 1 electronic resource (24 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS120336 |
| 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 | Center for Devices and Radiological Health (U.S.) |
| Portion of title | Presenting risk information in prescription drug and medical device promotion |
| General note | "Center for Biologics Evaluation and Research (CBER)." |
| General note | "Center for Veterinary Medicine (CVM)." |
| General note | "Center for Devices and Radiological Health (CDRH)." |
| General note | "Draft guidance." |
| General note | "May 2009." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:R 49/5/DRAFT |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |