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E-REPORT
Title Guidance for clinical investigators, institutional review boards, and sponsors [electronic resource] : process for handling referrals to FDA under 21 CFR 50.54 : additional safeguards for children in clinical investigations.
Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [2006]

Copies/Volumes

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 Internet  Electronic Report    AVAILABLE
Description i, 9 p. : digital, PDF file.
Note Title from PDF title page (viewed on May 12, 2009).
"December 2006".
Mode of access: Internet at the FDA CBER web site. Address as of 5/12/09: http://www.fda.gov/cber/gdlns/childclininv.pdf ; current access is available via PURL.
Subject Medical research personnel -- Government policy -- United States.
Clinical trials -- Government policy -- United States.
Pediatrics -- Research -- Government policy -- United States.
Other Author United States. Food and Drug Administration.
Other Title Process for handling referrals to FDA under 21 CFR 50.54.
Additional safeguards for children in clinical investigations.