Points to consider in the manufacture and testing of monoclonal antibody products for human use.
| 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, [1997] |
| Description | 1 online resource (50 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS113624 |
| Subjects |
| General note | Title from title screen (viewed on June 9, 2009). |
| General note | "February 28, 1997". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography note | Includes bibliographical references (p. 49-50). |
| Technical details | Mode of access: Internet at the FDA web site. Address as of 6/9/09: http://www.fda.gov/downloads/BiologicsBloodVaccines/GuidanceComplianceRegulatoryInformation/OtherRecommendationsforManufacturers/UCM153182.pdf ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:M 75 |
Availability
| Library | Location | Call Number | Status | Item Actions |
|---|---|---|---|---|
| Electronic Resources | Access Content Online | ✔ Available |