United States · Bill · HR
H.R. 931 (114th)
HEAL Act
Introduced
12 February 2015
Last action
13 February 2015 · Referred
Status
Referred to the Subcommittee on Health.
Sponsors
Rep. DeLauro, Rosa L. [D-CT-3], Rep. Slaughter, Louise McIntosh [D-NY-25], Rep. Meng, Grace [D-NY-6], Rep. Ellison, Keith [D-MN-5], Rep. Grijalva, Raúl M. [D-AZ-7], Rep. DeFazio, Peter A. [D-OR-4], Del. Norton, Eleanor Holmes [D-DC-At Large], Rep. McCollum, Betty [D-MN-4]
Subjects
Healthcare
Source updated
12 August 2025
Summary
Helping Effective Antibiotics Last Act of 2015 or the HEAL Act This bill amends the Federal Food, Drug, and Cosmetic Act to allow the Food and Drug Administration (FDA) to approve an antibacterial drug or biological product that is intended to treat a serious or life-threatening condition only for treating a well-defined population of patients. To be approved, the antibacterial product must produce superior outcomes over available therapies in the well-defined patient population. A product approved by this pathway must include in its prescribing information the population of patients expected to benefit from using the product and the method for identifying members of that population. The FDA must require each product to have a risk evaluation and mitigation strategy. The Centers for Disease Control and Prevention must monitor changes to bacterial drug resistance and changes to patient outcomes caused by bacterial drug resistance. Upon approval of antibacterial products, the FDA must identify susceptibility test interpretive criteria (the drug concentrations where a type of bacteria is categorized as susceptible, intermediate, or resistant) and update the criteria as needed based upon evidence of changes in patient outcomes. To be eligible for an exclusivity period extension, a qualified infectious disease product must be demonstrated to produce superior outcomes over available therapies. The FDA must issue guidance on the development of target product profiles for antibacterial drugs.
This text is taken from the official record. PoliticalRepo does not editorialize.
Timeline
12 February 2015
Introduced
Referred to the House Committee on Energy and Commerce.
Source: IntroReferral
12 February 2015
Introduced
Introduced in House
Source: IntroReferral
12 February 2015
Introduced
Introduced in House
Source: IntroReferral
13 February 2015
Referred
Referred to the Subcommittee on Health.
Source: Committee
Votes
No vote records are attached yet.
Versions
- Introduced in House · 12 February 2015 · Download file
Documents
3 official files
Introduced in House (text)
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Introduced in House (text)
Introduced in House · EN · 12 February 2015
Introduced in House (PDF)
Introduced in House · EN · 12 February 2015
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Introduced in House
summary · EN · 12 February 2015
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Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.
Sponsors
- Rep. DeLauro, Rosa L. [D-CT-3] · D · Sponsor
- Rep. Slaughter, Louise McIntosh [D-NY-25] · D · Sponsor
- Rep. Meng, Grace [D-NY-6] · D · Sponsor
- Rep. Ellison, Keith [D-MN-5] · D · Cosponsor
- Rep. Grijalva, Raúl M. [D-AZ-7] · D · Cosponsor
- Rep. DeFazio, Peter A. [D-OR-4] · D · Cosponsor
- Del. Norton, Eleanor Holmes [D-DC-At Large] · D · Cosponsor
- Rep. McCollum, Betty [D-MN-4] · D · 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/114th-congress/house-bill/931
- Open data entity: https://api.congress.gov/v3/bill/114/hr/931
- us · 114-hr-931 · source updated 12 August 2025