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42 U.S.C. § 236 — Administration of grants in multigrant proj­ects; promulgation of regulations

Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 236 — Administration of grants in multigrant proj­ects; promulgation of regulations

For the purpose of facilitating the administration of, and expediting the carrying out of the purposes of, the programs established by subchapters V, VI, and VII,11 See References in Text note below. and sections 242b, 246(a), 246(b), 246(c), 246(d),1 and 246(e) 1 of this title in situations in which grants are sought or made under two or more of such programs with respect to a single project, the Secretary is authorized to promulgate regulations— (1) under which the administrative functions under such programs with respect to such project will be performed by a single administrative unit which is the administrative unit charged with the administration of any of such programs or is the administrative unit charged with the supervision of two or more of such programs; (2) designed to reduce the number of applications, reports, and other materials required under such programs to be submitted with respect to such project, and otherwise to simplify, consolidate, and make uniform (to the extent feasible), the data and information required to be contained in such applications, reports, and other materials; and (3) under which inconsistent or duplicative requirements imposed by such programs will be revised and made uniform with respect to such project; except that nothing in this section shall be construed to authorize the Secretary to waive or suspend, with respect to any such project, any requirement with respect to any of such programs if such requirement is imposed by law or by any regulation required by law.

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Stable record: federal_law:legal_authorities:record_usc_28e3f4213fa9ffc898bf9070
Source file: Laws/federal/codes/united-states-code/title-42/section-236-administration-of-grants-in-multigrant-projects-promulgation-of-regulati--4d9de4ef85.md
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Source location: Title 42, Chapter 6A, § 236; chapter-6a-public-health-service.md

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For the purpose of facilitating the administration of, and expediting the carrying out of the purposes of, the programs established by subchapters V, VI, and VII,11 See References in Text note below. and sections 242b, 246(a), 246(b), 246(c), 246(d),1 and 246(e) 1 of this title in situations in which grants are sought or made under two or more of such programs with respect to a single project, the Secretary is authorized to promulgate regulations— (1) under which the administrative functions under such programs with respect to such project will be performed by a single administrative unit which is the administrative unit charged with the administration of any of such programs or is the administrative unit charged with the supervision of two or more of such programs; (2) designed to reduce the number of applications, reports, and other materials required under such programs to be submitted with respect to such project, and otherwise to simplify, consolidate, and make uniform (to the extent feasible), the data and information required to be contained in such applications, reports, and other materials; and (3) under which inconsistent or duplicative requirements imposed by such programs will be revised and made uniform with respect to such project; except that nothing in this section shall be construed to authorize the Secretary to waive or suspend, with respect to any such project, any requirement with respect to any of such programs if such requirement is imposed by law or by any regulation required by law.

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 301 — Short title

This chapter may be cited as the Federal Food, Drug, and Cosmetic Act.

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 301

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 360aa — Recommendations for investigations of drugs for rare diseases or conditions

**(a) Request by sponsor; response by Secretary** The sponsor of a drug for a disease or condition which is rare in the States may request the Secretary to provide written recommendations for the non-clinical and clinical investigations which must be conducted with the drug before— (1) it may be approved for such disease or condition under [section 355 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section355&num=0&edition=prelim), or (2) if the drug is a biological product, it may be licensed for such disease or condition under [section 262 of title 42](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section262&num=0&edition=prelim). If the Secretary has reason to believe that a drug for which a request is made under this section is a drug for a disease or condition which is rare in the States, the Secretary shall provide the person making the request written recommendations for the non-clinical and clinical investigations which the Secretary believes, on the basis of information available to the Secretary at the time of the request under this section, would be necessary for approval of such drug for such disease or condition under [section 355 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section355&num=0&edition=prelim) or licensing of such drug for such disease or condition under [section 262 of title 42](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section262&num=0&edition=prelim). **(b) Regulations** The Secretary shall by regulation promulgate procedures for the implementation of subsection (a).

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 360aa

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 10821 — Applications

**(a) Submission for allotment; contents** No allotment may be made under this subchapter to an eligible system unless an application therefor is submitted to the Secretary. Each such application shall contain— (1) assurances that amounts paid to such system from an allotment under this subchapter will be used to supplement and not to supplant the level of non-Federal funds available in the State in which such system is established to protect and advocate the rights of individuals with mental illness; (2) assurances that such system will have a staff which is trained or being trained to provide advocacy services to individuals with mental illness and to work with family members of clients served by the system where the individuals with mental illness are minors, legally competent and do not object, and legally incompetent and the legal guardians, conservators, or other legal representatives are family members; (3) assurances that such system, and any State agency or nonprofit organization with which such system may enter into a contract under [section 10804(a) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section10804/a&num=0&edition=prelim), will not, in the case of any individual who has a legal guardian, conservator, or representative other than the State, take actions which are duplicative of actions taken on behalf of such individual by such guardian, conservator, or representative unless such guardian, conservator, or representative requests the assistance of such system; and (4) such other information as the Secretary may by regulation prescribe. **(b) Satisfaction of requirements regarding trained staff** The assurance required under subsection (a)(2) regarding trained staff may be satisfied through the provision of tra

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 10821

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 10826 — Administration

**(a) In general** The Secretary shall carry out this subchapter through the Administrator of the Substance Abuse and Mental Health Services Administration. **(b) Regulations** Not later than 6 months after November 27, 1991, the Secretary shall promulgate final regulations to carry out this subchapter and subchapter III.

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 10826

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 242f to 242j — Transferred

### Statutory Notes #### Codification Section 242f, act July 1, 1944, ch. 373, title III, § 308, as added July 12, 1960, Pub. L. 86–610, § 3, 74 Stat. 364, which related to international cooperation with respect to biomedical research and health services research and statistical activities, was renumbered section 307 of act July 1, 1944, by Pub. L. 93–353 and transferred to section 242l of this title. Section 242g, act July 1, 1944, ch. 373, title III, § 309, as added Sept. 8, 1960, Pub. L. 86–720, § 1(a), 74 Stat. 819; amended Aug. 27, 1964, Pub. L. 88–497, § 3, 78 Stat. 613; Nov. 3, 1966, Pub. L. 89–749, § 4, 80 Stat. 1190; Dec. 5, 1967, Pub. L. 90–147, §§ 2(g), 8(c), 81 Stat. 534, 540; Aug. 16, 1968, Pub. L. 90–490, title III, § 302(a), 82 Stat. 788; Mar. 12, 1970, Pub. L. 91–208, §§ 1, 2, 84 Stat. 52; June 30, 1970, Pub. L. 91–296, title IV, § 401(b)(1)(B), 84 Stat. 352; June 18, 1973, Pub. L. 93–45, title I, § 104(b), (c), 87 Stat. 91, which related to graduate public health training grants, was renumbered section 313 of act July 1, 1944, by Pub. L. 93–353 and transferred to [section 245a of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section245a&num=0&edition=prelim), and was subsequently repealed. Section 242h, act July 1, 1944, ch. 373, title III, § 310, as added Sept. 25, 1962, Pub. L. 87–692, 76 Stat. 592, and amended and renumbered, which related to health services for domestic agricultural migrants, was renumbered section 319 of act July 1, 1944, by Pub. L. 93–353, title I, § 102(d), July 23, 1974, 88 Stat. 362, transferred to [section 247d of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section247d&num=0&edition=prelim), and subsequently renumbered and transferred to [section 254b o

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 242f to 242j

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 242q–1 — Membership

**(a) Composition** The Task Force shall be composed of— (1) the Assistant Secretary for Health; (2) the Surgeon General of the Public Health Service; (3) the Assistant Secretary for Planning and Evaluation; (4) the Director of the National Institute on Aging, and the Directors of such other agencies of the National Institutes of Health as the Secretary determines to be appropriate; (5) the Commissioner of the Administration on Aging; (6) the Commissioner of Food and Drugs; (7) the Under Secretary for Health of the Department of Veterans Affairs; (8) the Administrator of the the 11 So in original. Substance Abuse and Mental Health Services Administration; (9) the Administrator of the Centers for Medicare & Medicaid Services; (10) the Commissioner of Social Security; (11) the Director of the Agency for Healthcare Research and Quality; (12) two Members of the House of Representatives appointed by the Speaker of the House in consultation with the Minority Leader, and two members of the Senate appointed by the Majority Leader in consultation with the Minority Leader, not more than one of whom from each body shall be members of the same political party; and (13) three members of the general public, to be appointed by the Secretary, that shall include one representative each from— (A) a nonprofit group representing older Americans; (B) a private voluntary health organization concerned with the health problems affecting older Americans; and (C) a nonprofit organization concerned with research related to the health and independence of older Americans. **(b) Chair** The Secretary, acting through either the Assistant Secretary for Health or the Director of the National Institute on Aging, shall serve as the Chair of the Task Force. **(c) Quorum** A majorit

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 242q–1

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 280c–6 — Projects to improve maternal, infant, and child health

**(a) In general** (1) **Establishment of program** — The Secretary, acting through the Administrator of the Health Resources and Services Administration, shall make grants to eligible entities to pay the Federal share of the cost of providing the services specified in subsection (b) to families in which a member is— (A) a pregnant woman at risk of delivering an infant with a health or developmental complication; or (B) a child less than 3 years of age— (i) who is experiencing or is at risk of a health or developmental complication, or of child abuse or neglect; or (ii) who has been prenatally exposed to maternal substance abuse. (2) **Minimum period of awards; administrative consultations** (A) The Secretary shall award grants under paragraph (1) for periods of at least three years. (B) The Administrator of the Administration for Children, Youth, and Families and the Director of the National Commission to Prevent Infant Mortality shall be consulted regarding the promulgation of program guidelines and funding priorities under this section. (3) **Requirement of status as medicaid provider** (A) Subject to subparagraph (B), the Secretary may make a grant under paragraph (1) only if, in the case of any service under such paragraph that is covered in the State plan approved under title XIX of the Social Security Act [[42 U.S.C. 1396](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section1396&num=0&edition=prelim) et seq.] for the State involved— (i) the entity involved will provide the service directly, and the entity has entered into a participation agreement under the State plan and is qualified to receive payments under such plan; or (ii) the entity will enter into an agreement with an organization under which t

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 280c–6

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 281 — Organization of National Institutes of Health

**(a) Relation to Public Health Service** The National Institutes of Health is an agency of the Service. **(b) National research institutes and national centers** The following agencies of the National Institutes of Health are national research institutes or national centers: (1) The National Cancer Institute. (2) The National Heart, Lung, and Blood Institute. (3) The National Institute of Diabetes and Digestive and Kidney Diseases. (4) The National Institute of Arthritis and Musculoskeletal and Skin Diseases. (5) The National Institute on Aging. (6) The National Institute of Allergy and Infectious Diseases. (7) The Eunice Kennedy Shriver National Institute of Child Health and Human Development. (8) The National Institute of Dental and Craniofacial Research. (9) The National Eye Institute. (10) The National Institute of Neurological Disorders and Stroke. (11) The National Institute on Deafness and Other Communication Disorders. (12) The National Institute on Alcohol Abuse and Alcoholism. (13) The National Institute on Drug Abuse. (14) The National Institute of Mental Health. (15) The National Institute of General Medical Sciences. (16) The National Institute of Environmental Health Sciences. (17) The National Institute of Nursing Research. (18) The National Institute of Biomedical Imaging and Bioengineering. (19) The National Human Genome Research Institute. (20) The National Library of Medicine. (21) The National Center for Advancing Translational Sciences. (22) The John E. Fogarty International Center for Advanced Study in the Health Sciences. (23) The National Center for Complementary and Integrative Health. (24) The National Institute on Minority Health and Health Disparities. (25) Any other national center that, as an agency separate from

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 281

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 282 — Director of National Institutes of Health

**(a) Appointment** The National Institutes of Health shall be headed by the Director of NIH who shall be appointed by the President by and with the advice and consent of the Senate. The Director of NIH shall perform functions as provided under subsection (b) and as the Secretary may otherwise prescribe. **(b) Duties and authority** In carrying out the purposes of [section 241 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section241&num=0&edition=prelim), the Secretary, acting through the Director of NIH— (1) shall carry out this subchapter, including being responsible for the overall direction of the National Institutes of Health and for the establishment and implementation of general policies respecting the management and operation of programs and activities within the National Institutes of Health; (2) shall coordinate and oversee the operation of the national research institutes, national centers, and administrative entities within the National Institutes of Health; (3) shall, in consultation with the heads of the national research institutes and national centers, be responsible for program coordination across the national research institutes and national centers, including conducting priority-setting reviews, to ensure that the research portfolio of the National Institutes of Health is balanced and free of unnecessary duplication, and takes advantage of collaborative, cross-cutting research; (4) shall assemble accurate data to be used to assess research priorities, including— (A) information to better evaluate scientific opportunity, public health burdens, and progress in reducing health disparities; and (B) data on study populations of clinical research, funded by or conducted at each national research institute and

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 282

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 284d — Definitions

**(a) Health service research** For purposes of this subchapter, the term “health services research” means research endeavors that study the impact of the organization, financing and management of health services on the quality, cost, access to and outcomes of care. Such term does not include research on the efficacy of services to prevent, diagnose, or treat medical conditions. **(b) Clinical research** As used in this subchapter, the term “clinical research” means patient oriented clinical research conducted with human subjects, or research on the causes and consequences of disease in human populations involving material of human origin (such as tissue specimens and cognitive phenomena) for which an investigator or colleague directly interacts with human subjects in an outpatient or inpatient setting to clarify a problem in human physiology, pathophysiology or disease, or epidemiologic or behavioral studies, outcomes research or health services research, or developing new technologies, therapeutic interventions, or clinical trials.

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 284d

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