Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · BILL · 118th Congress · S. 5517 (Introduced in Senate) — To provide for the establishment, within the Food and Drug Administration, of an Abraham Accords Office to promote an... · Sec. 2

Sec. 2. Establishment of Abraham Accords Office within Food and Drug Administration

685 words·~3 min read·/bill/118/s/5517/is/section-2

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

Chapter X of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 391 et seq. ) is amended by adding at the end the following: The Secretary, acting through the Commissioner of Food and Drugs, shall establish within the Food and Drug Administration an office, to be known as the Abraham Accords Office, to be headed by a director. Not later than 2 years after the date of enactment of this section, the Secretary shall— in consultation with the governments of Abraham Accords countries, establish the Abraham Accords Office in an Abraham Accords country; and assign to such Office such personnel of the Food and Drug Administration as the Secretary determines necessary to carry out the functions of the Office.
The Secretary, acting through the Director of the Abraham Accords Office, shall, not later than 30 days after the Abraham Accords Office is established— provide technical assistance to parties in Abraham Accords countries on oversight of good manufacturing practices and other issues relevant to manufacturing medical products that are regulated by the Food and Drug Administration; facilitate interactions between the Food and Drug Administration and interested parties in Abraham Accords countries, including by sharing relevant information regarding United States regulatory pathways with such parties; offer technical assistance regarding research, development, and manufacturing of drugs and devices to parties located in an Abraham Accords country that intend to file an application for approval, licensure, clearance, or authorization of such a drug or device under section 505, 510(k), 513(f)(2), or 515 of this Act or section 351 of the Public Health Service Act; and carry out other functions and activities as the Secretary determines to be necessary to carry out this section.
The Secretary, in consultation with the Secretary of State, may suspend, for a period of not more than 6 months, the application of any of the actions described in subsection
(b)or
(c)with respect to an Abraham Accords country if the Secretary determines, and reports to the appropriate congressional committees, that— the exercise of such waiver authority would further the purposes of this section; or such a suspension is necessary to protect the national security interests of the United States. The Secretary, in consultation with the Secretary of State, may renew a waiver under paragraph
(1)for an additional period of not more than 6 months, not later than 15 days before the initial waiver expires, if the Secretary makes an additional determination and report described in paragraph (1). In this section, the term Abraham Accords country means a country identified by the Department of State as having signed the Abraham Accords. This section shall cease to have force or effect on the date that is 12 years after the date on which the Abraham Accords Office is established under subsection (a). . Not later than 3 years after the date of enactment of this Act, the Secretary of Health and Human Services shall submit to the Congress a report on the Abraham Accords Office established under section 1015 of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a), including— an evaluation of— how such Office has made progress in ensuring that manufacturers in Abraham Accords countries comply with applicable requirements with respect to applications submitted for approval, licensure, clearance, or authorization of a drug or device under section 505, 510(k), 513(f)(2), or 515 of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 355 , 360(k), 360c(f)(2), 360e) or section 351 of the Public Health Service Act ( 42 U.S.C. 262 ); and a list of parties that such Office has assisted pursuant to section 1015(c) of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a), and the drugs and devices that such parties intend to be the subjects of an application described in clause (i); and recommendations for increasing and improving coordination between the Food and Drug Administration and entities in Abraham Accords countries. In this section, the term Abraham Accords country has the meaning given such term in section 1015 of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a).
Connectionstraces to 3
Citation graph
cites case law
Sec. 2
Establishment of Abraham Accords Office within Food and Drug Administration
Cites 3Cited by 0 across 0 sources
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.