42 U.S.C. § 283a. Annual reporting to increase interagency collaboration and coordination
- (a)(a)
Collaboration with other HHS agencies
On an annual basis, the Director of NIH shall submit to the Secretary a report on the activities of the National Institutes of Health involving collaboration with other agencies of the Department of Health and Human Services. - (b)(b)
Clinical trials
Each calendar year, the Director of NIH shall submit to the Commissioner of Food and Drugs a report that identifies each clinical trial that is registered during such calendar year in the databank of information established under section 282(i) of this title. - (c)(c)
Human tissue samples
On an annual basis, the Director of NIH shall submit to the Congress a report that describes how the National Institutes of Health and its agencies store and track human tissue samples. - (d)(d)
First report
The first report under subsections (a), (b), and (c) shall be submitted not later than 1 year after January 15, 2007.
(July 1, 1944, ch. 373, title IV, § 403A, as added Pub. L. 109–482, title I, § 104(a)(3), Jan. 15, 2007, 120 Stat. 3691.)