Guidance for industry and FDA staff : expedited review of premarket submissions for devices.
| Other author/creator | Center for Devices and Radiological Health (U.S.) |
| 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 Devices and Radiological Health : Center for Biologics Evaluation and Research, [2008] |
| Description | 12 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS111920 |
| Subject(s) |
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| Portion of title | Expedited review of premarket submissions for devices |
| General note | Title from PDF title page (viewed on Apr. 27, 2009). |
| General note | "February 29, 2008". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Technical details | Mode of access: Internet at the FDA CBER Web site. Address as of 4/27/09: http://www.fda.gov/cdrh/mdufma/guidance/108.pdf ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:R 32 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |