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) 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) 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) First report
The first report under subsections (a), (b), and (c) shall be submitted not later than 1 year after January 15, 2007.
A prior section 403A of act July 1, 1944, was renumbered section
403D and is classified to section
283a–3 of this title.
Section applicable only with respect to amounts appropriated for fiscal year 2007 or subsequent fiscal years, see section 109 ofPub. L. 109–482, set out as an Effective Date of 2007 Amendment note under section
281 of this title.
The table below lists the classification updates, since Jan. 3, 2012, for this section. Updates to a broader range of sections may be found at the update page for containing chapter, title, etc.
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