End COVID Tyranny Act
A BILL
To reform the Centers for Disease Control and Prevention, limit the scope of public health authorities, and for other purposes.
Sec. 2 Sense of Congress
Sec. 3 Prohibitions on imposing a mask mandate in education settings
“(f) Nothing in this section authorizes the Secretary to require individuals to comply with a mask mandate (as defined in section 2(a) of the End COVID Tyranny Act) in any facility of a Head Start program (as defined in such section 2(a)) in response to a public health emergency declared under section 319 during the applicable period (as defined in such section 2(a)).”
Sec. 4 Appointment and authority of the Director of the Centers for Disease Control and Prevention; terms of CDC and NIH directors
Sec. 5 Limiting the CDC strategic plan
Sec. 6 Advisory committee to the CDC Director
“(A) Three members shall be appointed by the Secretary of Health and Human Services—
“(i) 1 of whom shall be appointed to represent the Department of Health and Human Services; and
“(ii) 1 of whom shall be a public health official.
“(B) Two members shall be appointed by the majority leader of the Senate.
“(C) Two members shall be appointed by the minority leader of the Senate.
“(D) Two members shall be appointed by the Speaker of the House of Representatives.
“(E) Two members shall be appointed by the minority leader of the House of Representatives.
“(F) Four members shall be appointed by the Comptroller General of the United States.”
Sec. 7 Limiting the scope of regulations of the Department of Health and Human Services to control communicable diseases
“(a) To prevent the introduction, transmission, or spread of communicable diseases from foreign countries into the States or possessions, or from one State or possession into any other State or possession, the Secretary may make and enforce regulations for the inspection, fumigation, disinfection, sanitation, pest extermination, or destruction of animals or articles found to be so infected or contaminated as to be sources of dangerous infection to human beings.”
Sec. 8 Eligibility for organ transplantation
“(4) Clarification regarding COVID–19 vaccination status—The criteria and standards established under paragraph (2) may not include any consideration of the COVID–19 vaccination status of organ donors or recipients, or of the incidence of COVID–19 positive rates in a geographic area or region, as determined by public health officials.”
Sec. 9 Congressional approval for public health emergencies
Sec. 10 Hospital visitation
“(9) has written policies and procedures regarding the visitation rights of individuals receiving items and services at the institution, which shall include—
“(A) a description of any clinically necessary or reasonable restriction or limitation that such institution may need to place on such rights and the reasons for the clinical restriction or limitation; and
“(B) a requirement that such institution inform each such individual of—
“(i) the right, subject to the individual’s consent, to receive the visitors whom the individual designates, including a spouse, another family member, or a friend; and
“(ii) the individual’s right to withdraw or deny such consent at any time; and”
Sec. 11 Foreign laboratory inspections and certification
“(f) Inspection and certification of foreign laboratories
“(1) In general—As a condition of eligibility to perform research involving animals under a grant, contract, or cooperative agreement administered by the National Institutes of Health or any national research institute, a laboratory located outside the United States that receives Federal funds shall be subject to quarterly inspections to evaluate compliance with the requirements under this title.
“(2) Inspection and certification requirements
“(A) Quarterly inspection process—The Secretary, in consultation with appropriate foreign regulatory authorities and international organizations, shall establish and implement a process for conducting quarterly inspections of foreign laboratories that have received an Animal Welfare Assurance (as defined in section 9.2 of title 42, Code of Federal Regulations) to ensure their continued compliance with the requirements under this title.
“(B) Assurances—The inspection process established by the Secretary pursuant to subparagraph (A) shall evaluate the compliance of foreign laboratories with the requirements under subsection (c)(1), including—
“(i) the establishment and operation of animal care committees;
“(ii) the review and evaluation of animal care and treatment; and
“(iii) proper record-keeping and reporting procedures.
“(3) Certification of compliance and public access
“(A) Issuance—Following each quarterly inspection required under paragraph (2), the inspecting authority shall issue a certification of compliance to the laboratories determined to be in compliance with the requirements under paragraph (2)(B).
“(B) Public access—Copies of the certificates of compliance issued pursuant to subparagraph (A) shall be maintained by the Office of Laboratory Animal Welfare and shall remain publicly accessible with other information about currently issued Animal Welfare Assurances.
“(C) Corrective action—Laboratories that fail to comply with the requirements under paragraph (2)(B) shall be given a reasonable opportunity to take corrective action.
“(4) Suspension or revocation of grant or contract for non-compliant foreign laboratories—If the Secretary determines that a foreign facility is not in compliance with the requirements under subsection (c)(1) and does not take appropriate corrective action after given a reasonable opportunity to do so, the Secretary shall suspend or revoke the applicable grant, contract, or cooperative agreement involving research on animals under such conditions as the Director of NIH determines appropriate, in accordance with subsection (d).
“(5) Designation of inspecting authority—The Secretary, in consultation with the Director of NIH, shall designate an appropriate authority to conduct the quarterly inspections required under paragraph (2) and issue certifications of compliance in accordance with paragraph (3).
“(6) Coordination with foreign authorities—The Secretary and the Director of NIH shall coordinate with appropriate foreign regulatory authorities and enter into agreements with foreign governments, as needed, to facilitate the implementation and enforcement of this subsection while respecting the sovereignty and laws of foreign nations.”