United States · Bill · HR
H.R. 1715 (111th)
Protection for Participants in Research Act of 2009
Introduced
25 March 2009
Last action
26 March 2009 · Referred
Status
Referred to the Subcommittee on Health.
Sponsors
Rep. DeGette, Diana [D-CO-1], Rep. Doggett, Lloyd [D-TX-37], Michael Burgess
Subjects
Healthcare, Education
Source updated
14 August 2025
Summary
Protection for Participants in Research Act of 2009 - Amends the Public Health Service Act to require all human subject research conducted, supported, or otherwise subject to federal regulation, to be conducted in accordance with the Common Rule and the vulnerable-population rules, as set forth in the Code of Federal Regulations. Requires the Secretary of Health and Human Services to review and harmonize such regulations. Requires informed consent before an individual may be a subject of human research. Requires an Institutional Review Board to approve all human subject research proposals. Directs the Secretary to establish criteria for determining whether a human subject research project must be conducted in accordance with a data safety and monitoring plan. Prohibits grants or awards to a public entity or private academic institution that does not have a program to educate investigators and Board members on the protection of human research subjects. Prohibits the use of federal funds for classified human subject research if: (1) the Board has waived the informed consent requirement; or (2) the research is exempt from Board review. Establishes the Office of Human Research Protections within the Office of the Secretary. Requires the Director of the Office to: (1) provide for the protection of human research subjects; (2) establish criteria regarding assurance of compliance with Common Rule requirements; and (3) coordinate federal activities with respect to the protection of human research subjects. Authorizes the Director to make grants for a model education program. Requires the Secretary to: (1) promulgate regulations enhancing the protection of people with diminished decision-making capacity participating in human subject research; and (2) study whether the number of certain members of Institutional Review Boards should be increased.
This text is taken from the official record. PoliticalRepo does not editorialize.
Timeline
25 March 2009
Introduced
Referred to the House Committee on Energy and Commerce.
Source: IntroReferral
25 March 2009
Introduced
Introduced in House
Source: IntroReferral
25 March 2009
Introduced
Introduced in House
Source: IntroReferral
26 March 2009
Referred
Referred to the Subcommittee on Health.
Source: Committee
Votes
No vote records are attached yet.
Versions
- Introduced in House · 25 March 2009 · Official file
Documents
3 official files
Introduced in House (text)
Introduced in House (text)
Introduced in House · EN · 25 March 2009
Introduced in House (PDF)
Introduced in House · EN · 25 March 2009
Introduced in House
summary · EN · 25 March 2009
Sponsors
- Rep. DeGette, Diana [D-CO-1] · D · Sponsor
- Rep. Doggett, Lloyd [D-TX-37] · D · Cosponsor
- Michael Burgess · R · Cosponsor
- · hsif00 · Standing
Related records
No cross-record relationships stored yet.
Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/111th-congress/house-bill/1715
- Open data entity: https://api.congress.gov/v3/bill/111/hr/1715
- us · 111-hr-1715 · source updated 14 August 2025