Guidance for industry : E 11 clinical investigation of medicinal products in the pediatric population.
Other author/creator | Center for Drug Evaluation and Research (U.S.) |
Other author/creator | Center for Biologics Evaluation and Research (U.S.) |
Other author/creator | International Conference on Harmonisation. |
Format | Electronic and Book |
Publication Info | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2000] |
Description | 14 p. : digital, PDF file |
Supplemental Content | https://purl.fdlp.gov/GPO/LPS113969 |
Subject(s) |
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Portion of title | E 11 clinical investigation of medicinal products in the pediatric population |
Portion of title | Clinical investigation of medicinal products in the pediatric population |
General note | Title from PDF title page (viewed on June 22, 2009). |
General note | "ICH". |
General note | "December 2000". |
General note | GPO Cataloging Record Distribution Program (CRDP). |
Technical details | Mode of access: Internet at the FHA web site. Address as of 6/22/09: http://www.fda.gov/downloads/RegulatoryInformation/Guidances/ucm129477.pdf ; current access is available via PURL. |
GPO item number | 0499-T (online) |
Govt. docs number | HE 20.4702:C 61/2 |
Available Items
Library | Location | Call Number | Status | Item Actions | |
Joyner | Electronic Resources | Access Content Online | ✔ Available |