Abraham Accords Office
In general
Office
Not later than 2 years after
in consultation with the governments of Abraham Accords countries, as well as appropriate United States Government diplomatic and security personnel—
select the location of the Abraham Accords Office in an Abraham Accords country; and
establish such office; and
assign to such office such personnel of the Food and Drug Administration as the Secretary determines necessary to carry out the functions of such office.
Duties
The Secretary, acting through the Director of the Abraham Accords Office, shall—
after the Abraham Accords Office is established—
as part of the Food and Drug Administration’s work to strengthen the international oversight of regulated commodities, provide technical assistance to regulatory partners in Abraham Accords countries on strengthening regulatory oversight and converging regulatory requirements for the oversight of regulated products, including good manufacturing practices and other issues relevant to manufacturing medical products that are regulated by the Food and Drug Administration; and
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, and facilitate feedback on the research, development, and manufacturing of products regulated in accordance with this chapter; and
carry out other functions and activities as the Secretary determines to be necessary to carry out this section.