Sound Science Act of 2026
A BILL
To amend the Toxic Substances Control Act to improve transparency of the regulatory process and coordination of science among Federal agencies, and for other purposes.
Sec. 2 Testing
“(i) the contents of the plan”
“(ii) the test methods and strategies proposed to be identified pursuant to subparagraph (C) for inclusion on the list under such subparagraph;”
Sec. 3 Consistency among existing requirements and among Federal department risk information
“(ii) consider—
“(I) only hazards and exposures that are more likely than not to result in an unreasonable risk of injury to health or the environment;
“(II) sentinel exposures to the chemical substance; and
“(III) aggregate exposures only if the Administrator issues a written determination that such consideration is necessary to provide greater clarity or precision in the risk evaluation;”
“(vi) consider any exposure limits or thresholds relating to the chemical substance developed by another Federal department or agency under any applicable law or regulation; and
“(vii) not assume noncompliance with any such applicable law or regulation relating to the chemical substance, including any occupational safety and health standard promulgated under section 6 of the Occupational Safety and Health Act of 1970 (29 U.S.C. 655) relating to the chemical substance.”
“(I) Interagency review—In conducting a risk evaluation under this subsection, the Administrator shall provide a process for Federal departments and agencies to submit information and feedback on critical uses, alternatives, and supply chain impacts, including by providing not less than 30 days to submit comments on the draft risk evaluation prior to providing public notice and an opportunity for comment in accordance with subparagraph (H).”
“(B) Selecting requirements—In selecting among requirements under subsection (a), the Administrator shall—
“(i) factor in, to the extent practicable—
“(I) the considerations under subparagraph (A), in accordance with subsection (a); and
“(II) any occupational safety and health standards promulgated under section 6 of the Occupational Safety and Health Act of 1970 (29 U.S.C. 655) relating to the chemical substance; and
“(ii) select those requirements that, to the extent applicable—
“(I) are cost-effective in relation to the minimization of the unreasonable risk; and
“(II) do not result in the creation of greater risks for health or the environment.”
Sec. 4 Improving accountability of final agency actions
Sec. 5 Strengthening scientific standards
“(6) if the Administrator is relying on the scientific standards described in this subsection or the weighting described in subsection (i), the extent to which any draft or final scientific assessment or risk evaluation developed by the Administrator is consistent with those standards or that weighting;
“(7) to the extent that the Administrator establishes any worker protection standards, the results of consultations with—
“(A) other Federal departments and agencies, including the Occupational Safety and Health Administration; and
“(B) to evaluate the need for a unique worker protection standard established by the Administrator, trained experts in industrial hygiene, toxicology, engineering, and process safety (including industry experts); and
“(8) the comments and expertise of other Federal departments and agencies, as provided pursuant to the interagency review process required under section 6(b)(4)(F)(viii), including the Department of Defense, the Department of Energy, the Occupational Safety and Health Administration, and the Department of Agriculture.”
“(5) Committee review
“(A) In-person peer review—When reviewing a risk evaluation carried out under section 6(b), the Committee shall conduct a complete in-person peer review.
“(B) Period of review—In carrying out subparagraph (A), the Committee shall provide a period of not less than 30 days to allow reviewers—
“(i) to conduct peer reviews; and
“(ii) to ensure a thorough review of—
“(I) the risk evaluation, including the underlying science relied on by the Administration and the risk determinations of the Administrator; and
“(II) the quality and scientific veracity of any draft or final scientific assessment relied on by the Administrator in conducting the risk evaluation.”