21 C.F.R. · Food and Drugs
21 C.F.R. § 50.52

Clinical investigations involving greater than minimal risk but presenting the prospect of direct benefit to individual subjects.

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Regulatory Text

21 C.F.R. § 50.52 — Clinical investigations involving greater than minimal risk but presenting the prospect of direct benefit to individual subjects.

§ 50.52 Clinical investigations involving greater than minimal risk but presenting the prospect of direct benefit to individual subjects. Any clinical investigation within the scope described in §§ 50.1 and 56.101 of this chapter in which more than minimal risk to children is presented by an intervention or procedure that holds out the prospect of direct benefit for the individual subject, or by a monitoring procedure that is likely to contribute to the subject's well-being, may involve children as subjects only if the IRB finds that: (a) The risk is justified by the anticipated benefit to the subjects; (b) The relation of the anticipated benefit to the risk is at least as favorable to the subjects as that presented by available alternative approaches; and (c) Adequate provisions are made for soliciting the assent of the children and permission of their parents or guardians as set forth in § 50.55. [66 FR 20598, Apr. 24, 2001, as amended at 78 FR 12951, Feb. 26, 2013]

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 50.52
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The regulatory text of 21 C.F.R. § 50.52 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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