Guidance for industry : MedWatch form FDA 3550A, mandatory reporting of adverse reactions related to human cells, tissues, and cellular and tissue-based products (HCT/Ps).
| 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 Biologics Evaluation and Research, [2005] |
| Description | i, 8 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS112829 |
| Subjects |
| Portion of title | MedWatch form FDA 3550A |
| Portion of title | Mandatory reporting of adverse reactions related to human cells, tissues, and cellular and tissue-based products (HCT/Ps) |
| General note | Title from PDF title page (viewed on May 19, 2009). |
| General note | "November 2005". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Technical details | Mode of access: Internet at the FDA CBER web site. Address as of 5/19/09: http://www.fda.gov/cber/gdlns/advhctp.htm ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:M 46 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |