Guidance for industry : changes to an approved application : biological products, human blood and blood components intended for transfusion or for further manufacture.
| Other author/creator | Center for Biologics Evaluation and Research (U.S.) |
| Format | Electronic and Book |
| Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2001] |
| Description | i, 30 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS113200 |
| Subject(s) |
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| Portion of title | Changes to an approved application |
| Portion of title | Biological products, human blood and blood components intended for transfusion or for further manufacture |
| General note | Title from PDF title page (viewed on May 28, 2009). |
| General note | "July 2001". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography note | Includes bibliographical references (p. 25-26). |
| Technical details | Mode of access: Internet at the FDA CBER web site. Address as of 5/28/09: http://www.fda.gov/cber/gdlns/bldchanges.pdf ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:B 52/4 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |