Title 42 › CHAPTER 6A — PUBLIC HEALTH SERVICE › SUBCHAPTER III — NATIONAL RESEARCH INSTITUTES › Part E — Other Agencies of NIH › subpart 1 — national center for advancing translational sciences › § 287a–2
The Director of the Office of Rare Diseases can give grants or make cooperative agreements with public or private nonprofit groups to plan, start, strengthen, and support regional centers that do clinical research, training, and demonstrations for diagnosing, preventing, controlling, and treating rare diseases. These awards must follow policies set by the Director of the National Institutes of Health. The Director must also coordinate these activities with other NIH institutes, centers, and the Food and Drug Administration when their work is related to rare diseases. Federal money can be used for staff, administration, and basic running costs (including patient care needed for research), clinical training and continuing education for health workers, public information, and clinical research and demonstration projects. Support may last up to 5 years and can be renewed for additional periods of up to 5 years if a scientific peer review panel created by the Director reviews the center and recommends renewal.
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The Public Health and Welfare, Source: USLM XML via OLRC
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42 U.S.C. § 287a–2
Title 42, The Public Health and Welfare
Last Updated
Sep 22, 2026
Release point: 119-110