Meeting the Demand for Pediatric Clinical Trials

被引：20

作者：

Connor, Edward M. ^{[1
,2
,3
]}

Smoyer, William E. ^{[4
,5
]}

Davis, Jonathan M. ^{[6
,7
]}

Zajicek, Anne ^{[8
]}

Ulrich, Linda ^{[9
]}

Purucker, Mary ^{[10
]}

Hirschfeld, Steven ^{[8
]}

机构：

[1] George Washington Univ, Dept Pediat, Washington, DC 20010 USA

[2] George Washington Univ, Clin & Translat Sci Inst, Washington, DC 20010 USA

[3] George Washington Univ, Sch Med & Hlth Sci, Washington, DC 20010 USA

[4] Ohio State Univ, Nationwide Childrens Hosp, Res Inst, Ctr Clin & Translat Res, Columbus, OH 43205 USA

[5] Ohio State Univ, Dept Pediat, Columbus, OH 43205 USA

[6] Tufts Med Ctr, Floating Hosp Children, Dept Pediat, Boston, MA 02111 USA

[7] Tufts Med Ctr, Floating Hosp Children, Tufts Clin & Translat Sci Inst, Boston, MA 02111 USA

[8] Eunice Kennedy Shriver NICHD, Bethesda, MD 20892 USA

[9] US FDA, Off Orphan Prod Dev, Silver Spring, MD 20993 USA

[10] NCATS, CTSA, Bethesda, MD 20892 USA

来源：

SCIENCE TRANSLATIONAL MEDICINE | 2014年 / 6卷 / 227期

关键词：

D O I：

10.1126/scitranslmed.3008043

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

High-quality, cost-ef ective pediatric clinical trials require a robust research and regulatory infrastructure and a properly trained workforce.

引用

页数：3

共 7 条

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[Anonymous], IOM CTSA REP

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[3]

[Anonymous], NICHD EFF HARM PED T

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