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42 U.S.C. § 290ee–3 — State demonstration grants for comprehensive opioid abuse response

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

42 U.S.C. § 290ee–3 — State demonstration grants for comprehensive opioid abuse response

**(a) Definitions** In this section: (1) **Dispenser** — The term “dispenser” has the meaning given the term in [section 802 of title 21](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section802&num=0&edition=prelim). (2) **Prescriber** — The term “prescriber” means a dispenser who prescribes a controlled substance, or the agent of such a dispenser. (3) **Prescriber of a schedule II, III, or IV controlled substance** — The term “prescriber of a schedule II, III, or IV controlled substance” does not include a prescriber of a schedule II, III, or IV controlled substance that dispenses the substance— (A) for use on the premises on which the substance is dispensed; (B) in a hospital emergency room, when the substance is in short supply; (C) for a certified opioid treatment program; or (D) in other situations as the Secretary may reasonably determine. (4) **Schedule II, III, or IV controlled substance** — The term “schedule II, III, or IV controlled substance” means a controlled substance that is listed on schedule II, schedule III, or schedule IV of [section 812(c) of title 21](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section812/c&num=0&edition=prelim). **(b) Grants for comprehensive opioid abuse response** (1) **In general** — The Secretary shall award grants to States, and combinations of States, to implement an integrated opioid abuse response initiative. (2) **Purposes** — A State receiving a grant under this section shall establish a comprehensive response plan to opioid abuse, which may include— (A) education efforts around opioid use, treatment, and addiction recovery, including education of residents, medical students, and physicians and other prescribers of schedule II, III, or IV controlled s

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Stable record: federal_law:legal_authorities:record_usc_31e7b4c43663389ef70937f6
Source file: Laws/federal/codes/united-states-code/title-42/section-290ee3-state-demonstration-grants-for-comprehensive-opioid-abuse-response--44e6fc16cd.md
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Source location: Title 42, Chapter 6A, § 290ee–3; chapter-6a-public-health-service.md

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**(a) Definitions** In this section: (1) **Dispenser** — The term “dispenser” has the meaning given the term in [section 802 of title 21](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section802&num=0&edition=prelim). (2) **Prescriber** — The term “prescriber” means a dispenser who prescribes a controlled substance, or the agent of such a dispenser. (3) **Prescriber of a schedule II, III, or IV controlled substance** — The term “prescriber of a schedule II, III, or IV controlled substance” does not include a prescriber of a schedule II, III, or IV controlled substance that dispenses the substance— (A) for use on the premises on which the substance is dispensed; (B) in a hospital emergency room, when the substance is in short supply; (C) for a certified opioid treatment program; or (D) in other situations as the Secretary may reasonably determine. (4) **Schedule II, III, or IV controlled substance** — The term “schedule II, III, or IV controlled substance” means a controlled substance that is listed on schedule II, schedule III, or schedule IV of [section 812(c) of title 21](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section812/c&num=0&edition=prelim). **(b) Grants for comprehensive opioid abuse response** (1) **In general** — The Secretary shall award grants to States, and combinations of States, to implement an integrated opioid abuse response initiative. (2) **Purposes** — A State receiving a grant under this section shall establish a comprehensive response plan to opioid abuse, which may include— (A) education efforts around opioid use, treatment, and addiction recovery, including education of residents, medical students, and physicians and other prescribers of schedule II, III, or IV controlled substances on relevant prescribing guidelines, the prescription drug monitoring program of the State described in subparagraph (B), and overdose prevention methods; (B) establishing, maintaining, or improving a comprehensive prescription drug monitoring program to track dispensing of schedule II, III, or IV controlled substances, which may— (i) provide for data sharing with other States; and (ii) allow all individuals authorized by the State to write prescriptions for schedule II, III, or IV controlled substances to access the prescription drug monitoring program of the State; (C) developing, implementing, or expanding prescription drug and opioid addiction treatment programs by— (i) expanding the availability of treatment for prescription drug and opioid addiction, including medication-assisted treatment and behavioral health therapy, as appropriate; (ii) developing, implementing, or expanding screening for individuals in treatment for prescription drug and opioid addiction for hepatitis C and HIV, and treating or referring those individuals if clinically appropriate; or (iii) developing, implementing, or expanding recovery support services and programs at high schools or institutions of higher education; (D) developing, implementing, and expanding efforts to prevent overdose death from opioid abuse or addiction to prescription medications and opioids; and (E) advancing the education and awareness of the public, providers, patients, consumers, and other appropriate entities regarding the dangers of opioid abuse, safe disposal of prescription medications, and detection of early warning signs of opioid use disorders. (3) **Application** — A State seeking a grant under this section shall submit to the Secretary an application in such form, and containing such information, as the Secretary may reasonably require. (4) **Use of funds** — A State that receives a grant under this section shall use the grant for the cost, including the cost for technical assistance, training, and administration expenses, of carrying out an integrated opioid abuse response initiative as outlined by the State’s comprehensive response plan to opioid abuse established under paragraph (2). (5) **Priority considerations** — In awarding grants under this section, the Secretary shall, as appropriate, give priority to a State that— (A) (i) provides civil liability protection for first responders, health professionals, and family members who have received appropriate training in administering a drug or device approved or cleared under the Federal Food, Drug, and Cosmetic Act [[21 U.S.C. 301](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section301&num=0&edition=prelim) et seq.] for emergency treatment of known or suspected opioid overdose; and (ii) submits to the Secretary a certification by the attorney general of the State that the attorney general has— (I) reviewed any applicable civil liability protection law to determine the applicability of the law with respect to first responders, health care professionals, family members, and other individuals who— (aa) have received appropriate training in administering a drug or device approved or cleared under the Federal Food, Drug, and Cosmetic Act for emergency treatment of known or suspected opioid overdose; and (bb) may administer a drug or device approved or cleared under the Federal Food, Drug, and Cosmetic Act for emergency treatment of known or suspected opioid overdose; and (II) concluded that the law described in subclause (I) provides adequate civil liability protection applicable to such persons; (B) has a process for enrollment in services and benefits necessary by criminal justice agencies to initiate or continue treatment in the community, under which an individual who is incarcerated may, while incarcerated, enroll in services and benefits that are necessary for the individual to continue treatment upon release from incarceration; (C) ensures the capability of data sharing with other States, where applicable, such as by making data available to a prescription monitoring hub; (D) ensures that data recorded in the prescription drug monitoring program database of the State are regularly updated, to the extent possible; (E) ensures that the prescription drug monitoring program of the State notifies prescribers and dispensers of schedule II, III, or IV controlled substances when overuse or misuse of such controlled substances by patients is suspected; and (F) has in effect one or more statutes or implements policies that maximize use of prescription drug monitoring programs by individuals authorized by the State to prescribe schedule II, III, or IV controlled substances. (6) **Evaluation** — In conducting an evaluation of the program under this section pursuant to section 701 of the Comprehensive Addiction and Recovery Act of 2016, with respect to a State, the Secretary shall report on State legislation or policies related to maximizing the use of prescription drug monitoring programs and the incidence of opioid use disorders and overdose deaths in such State. (7) **States with local prescription drug monitoring programs** (A) *In general* — In the case of a State that does not have a prescription drug monitoring program, a county or other unit of local government within the State that has a prescription drug monitoring program shall be treated as a State for purposes of this section, including for purposes of eligibility for grants under paragraph (1). (B) *Plan for interoperability* — In submitting an application to the Secretary under paragraph (3), a county or other unit of local government shall submit a plan outlining the methods such county or unit of local government shall use to ensure the capability of data sharing with other counties and units of local government within the state 11 So in original. Probably should be capitalized. and with other States, as applicable. **(c) Authorization of funding** For the purpose of carrying out this section, there are authorized to be appropriated $5,000,000 for each of fiscal years 2017 through 2021.

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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. § 802 — Definitions

As used in this subchapter: (1) The term “addict” means any individual who habitually uses any narcotic drug so as to endanger the public morals, health, safety, or welfare, or who is so far addicted to the use of narcotic drugs as to have lost the power of self-control with reference to his addiction. (2) The term “administer” refers to the direct application of a controlled substance to the body of a patient or research subject by— (A) a practitioner (or, in his presence, by his authorized agent), or (B) the patient or research subject at the direction and in the presence of the practitioner, whether such application be by injection, inhalation, ingestion, or any other means. (3) The term “agent” means an authorized person who acts on behalf of or at the direction of a manufacturer, distributor, or dispenser; except that such term does not include a common or contract carrier, public warehouseman, or employee of the carrier or warehouseman, when acting in the usual and lawful course of the carrier’s or warehouseman’s business. (4) The term “Drug Enforcement Administration” means the Drug Enforcement Administration in the Department of Justice. (5) The term “control” means to add a drug or other substance, or immediate precursor, to a schedule under part B of this subchapter, whether by transfer from another schedule or otherwise. (6) The term “controlled substance” means a drug or other substance, or immediate precursor, included in schedule I, II, III, IV, or V of part B of this subchapter. The term does not include distilled spirits, wine, malt beverages, or tobacco, as those terms are defined or used in subtitle E of the Internal Revenue Code of 1986. (7) The term “counterfeit substance” means a controlled substance which, or the container or labelin

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 802

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

21 U.S.C. § 1174, 1175 — Transferred

### Statutory Notes #### Codification Section 1174, Pub. L. 92–255, title IV, § 407, Mar. 21, 1972, 86 Stat. 78; Pub. L. 94–237, § 6(a), Mar. 19, 1976, 90 Stat. 244; Pub. L. 94–581, title I, § 111(c)(2), Oct. 21, 1976, 90 Stat. 2852, which prohibited discrimination against drug abusers by general hospitals, was redesignated section 526 of the Public Health Service Act by Pub. L. 98–24, § 2(b)(16)(B), Apr. 26, 1983, 97 Stat. 182, and is classified to [section 290ee–2 of Title 42](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section290ee–2&num=0&edition=prelim), The Public Health and Welfare. Section 1175, Pub. L. 92–255, title IV, § 408, Mar. 21, 1972, 86 Stat. 79; Pub. L. 93–282, title III, § 303(a), (b), May 14, 1974, 88 Stat. 137, 138; Pub. L. 94–237, § 4(c)(5)(A), (B), Mar. 19, 1976, 90 Stat. 244; Pub. L. 94–581, title I, § 111(c)(3), Oct. 21, 1976, 90 Stat. 2852; Pub. L. 97–35, title IX, § 973(d), Aug. 13, 1981, 95 Stat. 598, which related to confidentiality of patients’ records, was redesignated section 527 of the Public Health Service Act by Pub. L. 98–24, § 2(b)(16)(B), Apr. 26, 1983, 97 Stat. 182, and is classified to [section 290ee–3 of Title 42](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section290ee–3&num=0&edition=prelim).

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 1174, 1175

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

5 U.S.C. § 7361 — Drug abuse

**(a)** The Office of Personnel Management shall be responsible for developing, in cooperation with the President, with the Secretary of Health and Human Services (acting through the National Institute on Drug Abuse), and with other agencies, and in accordance with applicable provisions of this subchapter, appropriate prevention, treatment, and rehabilitation programs and services for drug abuse among employees. Such agencies are encouraged to extend, to the extent feasible, such programs and services to the families of employees and to employees who have family members who are drug abusers. Such programs and services shall make optimal use of existing governmental facilities, services, and skills. **(b)** Section 527 11 See References in Text note below. of the Public Health Service Act ([42 U.S.C. 290ee–3](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section290ee–3&num=0&edition=prelim)), relating to confidentiality of records, and any regulations prescribed thereunder, shall apply with respect to records maintained for the purpose of carrying out this section. **(c)** Each agency shall, with respect to any programs or services provided by such agency, submit such written reports as the Office may require in connection with any report required under [section 7363 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title5-section7363&num=0&edition=prelim). **(d)** For the purpose of this section, the term “agency” means an Executive agency.

Source: Supplied U.S. Code snapshot — release unconfirmed · 5 U.S.C. § 7361

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

21 U.S.C. § 301 — Short title

Page 30 TITLE 21—FOOD AND DRUGS § 301 Sec. 398. Notices to States regarding imported food. 399. Grants to enhance food safety. 399a. Office of the Chief Scientist. 399b. Office of Women’s Health. 399c. Improving the training of State, local, terri- torial, and tribal food safety officials. 399d. Employee protections. 399e. Nanotechnology. 399f. Ensuring adequate information regarding pharmaceuticals for all populations, par- ticularly underrepresented subpopulations, including racial subgroups. 399g. Food and Drug Administration Intercenter Institutes. 399h. National Centers of Excellence in Advanced and Continuous Pharmaceutical Manufac- turing. 399i. Food and Drug Administration Working Cap- ital Fund. SUBCHAPTER I—SHORT TITLE § 301. Short title This chapter may be cited as the Federal Food, Drug, and Cosmetic Act. (June 25, 1938, ch. 675, § 1, 52 Stat. 1040.) Statutory Notes and Related Subsidiaries EFFECTIVE DATE; POSTPONEMENT IN CERTAIN CASES Act June 23, 1939, ch. 242, §§ 1, 2, 53 Stat. 853, 854, pro- vided that: ‘‘[SEC. 1] (a) The effective date of the following provi- sions of the Federal Food, Drug, and Cosmetic Act is hereby postponed until January 1, 1940: Sections 402(c) [342(c) of this title]; 403(e)(1) [343(e)(1) of this title]; 403(g), (h), (i), (j), and (k) [343(g) to (k) of this title]; 501(a), (4) [351(a)(4) of this title]; 502(b), (d), (e), (f), (g), and (h) [352(b), (d) to (h) of this title]; 601(e) [361(e) of this title]; and 602(b) [362(b) of this title]. ‘‘(b) The Secretary of Agriculture shall promulgate regulations further postponing to July 1, 1940[,] the ef- fective date of the provisions of sections 403(e)(1) [343(e)(1) of this title]; 403(g), (h), (i), (j), and (k) [343(g) to (k)]; 502(b), (d), (

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