HR-2438 : Still Just a Bill

This bill requires the Food and Drug Administration to issue guidance that addresses using alternative statistical methods, including adaptive trial design and Bayesian methods, in clinical trials and in the development and review of drugs and biological products.

Action Timeline

Action DateTypeTextSource
2015-05-22CommitteeReferred to the Subcommittee on Health.House committee actions
2015-05-19IntroReferralReferred to the House Committee on Energy and Commerce.House floor actions
2015-05-19IntroReferralIntroduced in HouseLibrary of Congress

Sponsor :

Chris Collins [R] (NY-27)
See Cosponsors

Policy Area :

Health
See Subjects
  • Administrative law and regulatory procedures
  • Drug safety, medical device, and laboratory regulation
  • Medical research
  • Department of Health and Human Services
  • Food and Drug Administration (FDA)

Related Bills

See Related Bills