42 U.S.C. § 285e–9 — Alzheimer’s disease registry
submitted 82 years ago by Pub. L. 99-158 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 110 words · no verdicts yet
The Institute's Director may fund a registry tracking Alzheimer's disease cases. The registry collects data, tracks the disease's spread, and trains data collectors. Grant recipients must be medical or public health schools with a large, diverse patient base.
The Director* of the Institute may make a grant to develop a registry for the collection of epidemiological data about Alzheimer’s disease and its incidence in the United States, to train personnel in the collection of such data, and for other matters respecting such disease.
To qualify for a grant under subsection (a) an applicant shall—
be an accredited school of medicine or public health which has expertise in the collection of epidemiological data about individuals with Alzheimer’s disease and in the development of disease registries, and
have access to a large patient population, including a patient population representative of diverse ethnic backgrounds.
Source credit: (July 1, 1944, ch. 373, title IV, § 445G, formerly Pub. L. 99–158, § 12, Nov. 20, 1985, 99 Stat. 885; renumbered § 445G of act July 1, 1944, and amended Pub. L. 103–43, title VIII, § 801, June 10, 1993, 107 Stat. 163.)
- 1944Enacted · Pub. L. 99-158 · 99 Stat. 885
- 1944Amended · Pub. L. 103-43 · 107 Stat. 163
A history note hasn’t been published yet. The record shows enactment by Pub. L. 99-158 on 1944-07-01.
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