Sec. 773. ### (a)
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## SEC. 773 ###
(a)Fees derived from amounts assessed and collected for fiscal year 2026, credited under the heading “Department of Health and Human Services—Food and Drug Administration—Salaries and Expenses”, and made available for expenditure under such heading must comply with each provision contained in current user fee authorizations, appropriations Acts, and commitment letters, as transmitted from the Secretary of Health and Human Services to the chair and ranking member of the Committee on Health, Education, Labor, and Pensions of the Senate and the chair and ranking member of the Committee on Energy and Commerce of the House of Representatives regarding reauthorization of such current user fee authorizations: * Provided,* That the term current user fee authorizations means those user fees authorized at 21 U.S.C. 379h, 21 U.S.C. 379j, 21 U.S.C. 379j-42, 21 U.S.C. 379j-52, 21 U.S.C. 379j-12, 21 U.S.C. 379j-21, 21 U.S.C. 387s, 42 U.S.C. 263b, 21 U.S.C. 381, 21 U.S.C. 360n and 360ff, 21 U.S.C. 379-j31, 21 U.S.C. 379j-62 , 21 U.S.C. 353(e)(3), 21 U.S.C. 360eee-3(c)(1), 21 U.S.C. 384d(c)(8), 21 U.S.C. 360bbb-4a, and 21 U.S.C. 379j-72. ###
(b)####
(1)Not later than 90 days after the date of enactment of this Act, the Food and Drug Administration shall submit to the Committees on Appropriations of the House of Representatives and the Senate a report that includes obligation and outlay estimates and full-time equivalent
(FTE)personnel staffing estimates for fiscal year 2026 for each Food and Drug Administration program that uses both general fund appropriations and funds derived from user fees: * Provided,* That such report shall include a table with separate columns for general fund appropriations and funds derived from user fees for such obligations, outlays and FTE personnel staffing: * Provided further,* That such report shall be certified by the Ombudsman of the Food and Drug Administration. ####
(2)The report in paragraph
(1)shall be updated, certified by the Ombudsman of the Food and Drug Administration, and submitted to the Committees on Appropriations of the House of Representatives and the Senate not later than 45 days after each fiscal quarter until all such funds are expended: * Provided,* That a plan for such ongoing quarterly reporting shall be submitted with the report required by subsection (b)(1).
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Traces to 17 documents
U.S. Code
- Authority to assess and use drug fees§ 379h
- Authority to assess and use device fees§ 379j
- Authority to assess and use human generic drug fees§ 379j–42
- Authority to assess and use biosimilar biological product fees§ 379j–52
- Authority to assess and use animal drug fees§ 379j–12
- Authority to assess and use generic new animal drug fees§ 379j–21
- User fees§ 387s
- Certification of mammography facilities§ 263b
- Imports and exports§ 381
- Priority review to encourage treatments for tropical diseases§ 360n
- Confidential information§ 379
- Authority to assess and use outsourcing facility fees§ 379j–62
- Exemptions and consideration for certain drugs, devices, and biological products§ 353
- National standards for third-party logistics providers§ 360eee–3
- Accreditation of third-party auditors§ 384d
- Priority review to encourage treatments for agents that present national security threats§ 360bbb–4a
- Authority to assess and use OTC monograph fees§ 379j–72
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Sec. 773
### (a)
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