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42 U.S.C. § 285o–4 — Medication Development Program

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

42 U.S.C. § 285o–4 — Medication Development Program

**(a) Establishment** There is established in the Institute a Medication Development Program through which the Director of such Institute shall— (1) conduct periodic meetings with the Commissioner of Food and Drugs to discuss measures that may facilitate the approval process of drug abuse treatments; (2) encourage and promote (through grants, contracts, international collaboration, or otherwise) expanded research programs, investigations, experiments, community trials, and studies, into the development and use of medications to treat drug addiction; (3) establish or provide for the establishment of research facilities; (4) report on the activities of other relevant agencies relating to the development and use of pharmacotherapeutic treatments for drug addiction; (5) collect, analyze, and disseminate data useful in the development and use of pharmacotherapeutic treatments for drug addiction and collect, catalog, analyze, and disseminate through international channels, the results of such research; (6) directly or through grants, contracts, or cooperative agreements, support training in the fundamental sciences and clinical disciplines related to the pharmacotherapeutic treatment of drug abuse, including the use of training stipends, fellowships, and awards where appropriate; and (7) coordinate the activities conducted under this section with related activities conducted within the National Institute on Alcohol Abuse and Alcoholism, the National Institute of Mental Health, and other appropriate institutes and shall consult with the Directors of such Institutes. **(b) Duties** In carrying out the activities described in subsection (a), the Director of the Institute— (1) shall collect and disseminate through publications and other appropriate means, information per

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Stable record: federal_law:legal_authorities:record_usc_e4feffe2b0022fb4d263e17e
Source file: Laws/federal/codes/united-states-code/title-42/section-285o4-medication-development-program--9c3ef0052f.md
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Source location: Title 42, Chapter 6A, § 285o–4; chapter-6a-public-health-service.md

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**(a) Establishment** There is established in the Institute a Medication Development Program through which the Director of such Institute shall— (1) conduct periodic meetings with the Commissioner of Food and Drugs to discuss measures that may facilitate the approval process of drug abuse treatments; (2) encourage and promote (through grants, contracts, international collaboration, or otherwise) expanded research programs, investigations, experiments, community trials, and studies, into the development and use of medications to treat drug addiction; (3) establish or provide for the establishment of research facilities; (4) report on the activities of other relevant agencies relating to the development and use of pharmacotherapeutic treatments for drug addiction; (5) collect, analyze, and disseminate data useful in the development and use of pharmacotherapeutic treatments for drug addiction and collect, catalog, analyze, and disseminate through international channels, the results of such research; (6) directly or through grants, contracts, or cooperative agreements, support training in the fundamental sciences and clinical disciplines related to the pharmacotherapeutic treatment of drug abuse, including the use of training stipends, fellowships, and awards where appropriate; and (7) coordinate the activities conducted under this section with related activities conducted within the National Institute on Alcohol Abuse and Alcoholism, the National Institute of Mental Health, and other appropriate institutes and shall consult with the Directors of such Institutes. **(b) Duties** In carrying out the activities described in subsection (a), the Director of the Institute— (1) shall collect and disseminate through publications and other appropriate means, information pertaining to the research and other activities under this section; (2) shall make grants to or enter into contracts and cooperative agreements with individuals and public and private entities to further the goals of the program; (3) may, in accordance with [section 289e of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section289e&num=0&edition=prelim), and in consultation with the National Advisory Council on Drug Abuse, acquire, construct, improve, repair, operate, and maintain pharmacotherapeutic research centers, laboratories, and other necessary facilities and equipment, and such other real or personal property as the Director determines necessary, and may, in consultation with such Advisory Council, make grants for the construction or renovation of facilities to carry out the purposes of this section; (4) may accept voluntary and uncompensated services; (5) may accept gifts, or donations of services, money, or property, real, personal, or mixed, tangible or intangible; and (6) shall take necessary action to ensure that all channels for the dissemination and exchange of scientific knowledge and information are maintained between the Institute and the other scientific, medical, and biomedical disciplines and organizations nationally and internationally. **(c) Report** (1) **In general** — Not later than December 31, 1992, and each December 31 thereafter, the Director of the Institute shall submit to the Office of National Drug Control Policy established under section 1501 11 See References in Text note below. of title 21 a report, in accordance with paragraph (3), that describes the objectives and activities of the program assisted under this section. (2) **National Drug Control Strategy** — The Director of National Drug Control Policy shall incorporate, by reference or otherwise, each report submitted under this subsection in the National Drug Control Strategy submitted the following February 1 under section 1504 1 of title 21. **(d) “Pharmacotherapeutics” defined** For purposes of this section, the term “pharmacotherapeutics” means medications used to treat the symptoms and disease of drug abuse, including medications to— (1) block the effects of abused drugs; (2) reduce the craving for abused drugs; (3) moderate or eliminate withdrawal symptoms; (4) block or reverse the toxic effect of abused drugs; or (5) prevent relapse in persons who have been detoxified from drugs of abuse.

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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.

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 236

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

42 U.S.C. § 289e — Use of appropriations

**(a)** Appropriations to carry out the purposes of this subchapter, unless otherwise expressly provided, may be expended in the District of Columbia for— (1) personal services; (2) stenographic recording and translating services; (3) travel expenses (including the expenses of attendance at meetings when specifically authorized by the Secretary); (4) rental; (5) supplies and equipment; (6) purchase and exchange of medical books, books of reference, directories, periodicals, newspapers, and press clippings; (7) purchase, operation, and maintenance of passenger motor vehicles; (8) printing and binding (in addition to that otherwise provided by law); and (9) all other necessary expenses in carrying out this subchapter. Such appropriations may be expended by contract if deemed necessary, without regard to [section 6101 of title 41](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title41-section6101&num=0&edition=prelim). **(b)** (1) None of the amounts appropriated under this chapter for the purposes of this subchapter may be obligated for the construction of facilities (including the acquisition of land) unless a provision of this subchapter establishes express authority for such purpose and unless the Act making appropriations under such provision specifies that the amounts appropriated are available for such purpose. (2) Any grants, cooperative agreements, or contracts authorized in this subchapter for the construction of facilities may be awarded only on a competitive basis.

Source: Supplied U.S. Code snapshot — release unconfirmed · 42 U.S.C. § 289e

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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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