Guidance for industry : providing regulatory submissions to the Center for Biologics Evaluation and Research (CBER) in electronic format, lot release protocols.
| 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, [2007] |
| Description | i, 6 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS112107 |
| Subjects |
| Portion of title | Providing regulatory submissions to the Center for Biologics Evaluation and Research (CBER) in electronic format, lot release protocols |
| General note | Title from PDF title page (viewed on Apr. 30, 2009). |
| General note | No longer available via Internet. |
| General note | "November 2007". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Technical details | Mode of access: Internet at the FDA CBER web site. Address as of 4/30/09: http://www.fda.gov/cber/gdlns/elotrel.pdf ; current access is available via PURL. |
| Genre/form | Electronic records. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:R 26/4 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |