User fees and refunds for premarket approval applications.
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, [2009] |
Description | 9 p. : digital, PDF file |
Supplemental Content | https://purl.fdlp.gov/GPO/LPS110430 |
Subject(s) |
Click here for more information about this title
Variant title | At head of title: Draft guidance for industry and FDA staff |
General note | Title from title screen (viewed on Mar. 19, 2009). |
General note | "March 13, 2009". |
General note | GPO Cataloging Record Distribution Program (CRDP). |
Technical details | Mode of access: Internet at the FDA web site. Address as of 3/19/90: http://www.fda.gov/cdrh/ode/guidance/1681.pdf ; current access is available via PURL. |
GPO item number | 0499-T-02 (online) |
Govt. docs number | HE 20.4802:US 2 |
Available Items
Library | Location | Call Number | Status | Item Actions | |
Joyner | Electronic Resources | Access Content Online | ✔ Available |