Code of Federal Regulations · Section
§ 11.20 — Who Must Submit Clinical Trial Registration Information?
42 C.F.R. § 11.20
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The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.
Authorizing Statute
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Departmental regulations5 U.S.C. § 301
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Regulations42 U.S.C. § 216
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Director of National Institutes of Health42 U.S.C. § 282
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Research and investigations generally42 U.S.C. § 241
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National Library of Medicine42 U.S.C. § 286