In vitro diagnostic (IVD) device studies, frequently asked questions.
| 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, [2007] |
| Description | 1 online resource (ii, 46 p.) : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS112196 |
| Subject(s) |
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| Variant title | At head of title: Draft guidance for industry and FDA staff |
| General note | Title from PDF title page (viewed on May 4, 2009). |
| General note | "Document issued on: October 25, 2007". |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Bibliography note | Includes bibliographical references: (p. 30-32). |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:V 83/2/DRAFT |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |