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H.Res. 309

Expressing the sense of the House of Representatives that the Food and Drug Administration has the authority to approve drugs for abortion care.

This resolution expresses the sense of the House of Representatives that the Food and Drug Administration (FDA) has the authority to review and approve drugs pursuant to its own expertise, and that recent court decisions blocking the FDA's approval of mifepristone (which is used in medication abortion) violate congressional intent with respect to the FDA's authority.

Referred to the House Committee on Energy and Commerce.

Rep. Manning, Kathy E. [D-NC-6](D-NC)Sponsor
48 cosponsors48 D
48cosponsors1committees3actions
  1. IntroReferralH11100

    Referred to the House Committee on Energy and Commerce.

    Energy and Commerce Committee
  2. IntroReferralIntro-H

    Introduced in House

  3. IntroReferral1000

    Introduced in House

Expressing the sense of the House of Representatives that the Food and Drug Administration… — Informed