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H.R. 5187
U.S. House•In House Committee
Summary
H.R. 5187, to establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity, was introduced in the House on Sep 8, 2025 by Rep. Ro Khanna (D) with 2 co-sponsors. It was referred to Armed Services, and last saw action on Sep 8, 2025: Referred to the House Committee on Armed Services.
Record
Text
H.R. 5187 has 2 co-sponsors.
hb5187/introduced-in-house.txt119 HR 5187 IH: To establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity.U.S. House of Representatives2025-09-08text/xmlENPursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.I 119th CONGRESS 1st Session H. R. 5187 IN THE HOUSE OF REPRESENTATIVES September 8, 2025 Mr. Khanna (for himself, Mr. Garamendi , and Mr. Davis of North Carolina ) introduced the following bill; which was referred to the Committee on Armed Services A BILLTo establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity.1.Bioindustrial commercialization program(a)In generalNot later than one year after the date of the enactment of this Act, the Secretary of Defense may establish a program to support the expansion of the domestic capacity for bioindustrial manufacturing of critical biomanufactured products at a commercial level through awards to eligible entities for establishing, upgrading, and retooling of eligible bioindustrial manufacturing facilities.(b)Awards(1)In generalAn entity seeking an award under the program shall submit to the Secretary an application at such time, in such manner, and containing such information as the Secretary determines appropriate.(2)Competitive awardsThe Secretary shall make each award under the program to an eligible entity in a competitive manner.(3)Award criteriaIn selecting eligible entities to receive awards under the program, the Secretary shall consider the following criteria:(A)The potential of the technology of such eligible entity to improve domestic resilience and protect critical supply chains for critical biomanufactured products.(B)How the technology of such eligible entity could help meet the demand for the capabilities required by the next generation of warfighters.(C)The ability of the eligible bioindustrial manufacturing facility with respect to which such eligible entity is seeking such award to be repurposed and the range of products that such eligible bioindustrial manufacturing facility is capable of producing.(D)Whether the eligible bioindustrial manufacturing facility with respect to which such eligible entity is seeking such award supports the goal of wide geographic distribution of bioindustrial manufacturing facility across the United States.(E)Whether the eligible bioindustrial manufacturing facility with respect to which such eligible entity is seeking such award is located in geographic proximity to sources of input materials for the production of critical biomanufactured products or areas with established biomanfuacturing capabilities.(F)Such additional considerations that the Secretary deems appropriate.(4)Use of award fundsA recipient of an award under the program may use funds received under such award for the establishment, upgrading, or retooling of one or more eligible bioindustrial manufacturing facilities to produce critical biomanufactured products, including the development of business or technical plans related to such establishment, upgrading, or retooling.(c)OversightIf the Secretary establishes the program, the Secretary shall establish reporting requirements for recipients of awards under the program which shall include requirements for period reports on the following:(1)The progress of the recipient in establishing, upgrading, or retooling the eligible bioindustrial manufacturing facility with respect to which such recipient received such award.(2)The estimated timeline and funding requirements for the recipient to begin biomanufacturing at the eligible bioindustrial manufacturing facility described in paragraph (1).(3)The products, including the critical biomanufactured products, that are or will be produced at the eligible bioindustrial manufacturing facility described in paragraph (1).(4)The progress of the recipient in entering into an agreement with the Department of Defense or an element thereof to provide critical biomanufactured products, that are or will be produced at the eligible bioindustrial manufacturing facility described in paragraph (1) once such eligible bioindustrial manufacturing facility begins biomanufacturing.(d)Reports to Congress(1)Initial reportNot later than 90 days after the date of the enactment of this Act, the Secretary shall submit to the Committees on Armed Services of the House of Representatives and Senate a report on the plan of the Secretary for allocating amounts appropriated to the Department of Defense to fund the program.(2)Annual reportsNot later than one year after the date of the enactment of this Act, and annually thereafter, the Secretary shall submit to the Committees on Armed Services of the House of Representatives and Senate a report on the activities under the program, including—(A)a list of the awards made under the program as of the date on which the report is submitted, including, for each such award—(i)the name of the entity that received the award;(ii)the location of the eligible bioindustrial manufacturing facility with respect to which such entity received the award;(iii)the amount of the award, disaggregated by the initial amount of the award and any additional amounts provided under the award;(iv)an explanation of the criteria supporting making the award to such entity, including a description of any notable technologies of such entity relevant to the award;(v)if applicable, an explanation of the rational for providing additional amounts under the award; and(vi)to the extent practicable, and explanation of the effects of the award;(B)an identification of amounts available to the Department of Defense for making awards under the program as of the date on which the report is submitted and an explanation of any plans for the use of such amounts;(C)an explanation of the communication between the Secretary and eligible entities seeking an award under the program regarding requirements and timelines for such awards; and(D)an explanation of how the establishment, upgrading, or retooling of the eligible bioindustrial manufacturing facility for which awards were made under the program aligns with priorities and needs of the Department of Defense and national security.(e)Sunset(1)In generalExcept as provided by paragraph (2), this section shall terminate on the date that is 10 years after the date of the enactment of this Act.(2)ExtensionThe Secretary may change the date on which this section terminates to a date that is later than the date on which this section would terminate under paragraph (1) if the President determines that the continuation of the program is necessary to meet national economic and national security needs.(f)DefinitionsIn this section:(1)The term biomanufacturing means the utilization of biological systems to develop new and advance existing products, tools, and processes at commercial scale.(2)The term critical biomanufactured product means a chemical, material, and other product that is manufactured using biomanufacturing and is relevant to the Department of Defense.(3)The term eligible bioindustrial manufacturing facility means a bioindustrial manufacturing facility that—(A)is or, if not yet established, will be located in the United States; and(B)is or, pursuant to an award under the program, will produce critical biomanufactured products.(4)The term eligible entity means an entity that—(A)is a private entity;(B)applied for an award under the program in accordance with subsection (b)(1); and(C)meets such other criteria for eligibility for an award under the program as determined by the Secretary.(5)The term program means the program established under subsection (a).(6)The term Secretary means the Secretary of Defense.
Tracker
The tracker indicates the progress of this legislation as it moves through the legislative process.
- Introduced2025-09-08
- Passed House
- Passed Senate
- Conference
- To President
- Became Law
To establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity.
Sponsors
Rep. Ro Khanna (D) sponsors H.R. 5187, and 2 members have co-sponsored it, all of them from the day it was introduced.
Committees
H.R. 5187 went before 1 committee: Armed Services.
Actions
H.R. 5187 has taken 2 actions since Sep 8, 2025.
| Chamber | Action | |||
|---|---|---|---|---|
Sep 8, 2025 | House | Introduced in House | ||
Sep 8, 2025 | House | Referred to the House Committee on Armed Services.Armed Services Committee |
Votes
H.R. 5187 has not gone to a roll call.
Related bills
1 bill is related to H.R. 5187.
Titles
H.R. 5187 goes by 2 titles.
- To establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity. — Official Title as Introduced
- To establish in the Department of Defense a program to support the expansion of domestic bioindustrial manufacturing capacity. — Display Title
Lobbying
3 clients hired 2 firms and 5 registered lobbyists who named H.R. 5187 in 4 quarterly filings, 2025 to 2026. Reported under the Lobbying Disclosure Act; a filing’s income covers everything its registrant worked that quarter, so the amounts below are the filings’, not this bill’s.
Filed under Banking, Energy/Nuclear, Financial Institutions/Investments/Securities, Government Issues, Health Issues, Homeland Security, Housing, Immigration.
Clients
Who paid to be heard, by how many filings named the bill.
| Client | Business | State | Firms | Filings | Reported |
|---|---|---|---|---|---|
| REAL ESTATE ROUNDTABLE | — | District of Columbia | 1 | 2 | — |
| AGIOS PHARMACEUTICALS | Biotech/biopharmaceutical company | Massachusetts | 1 | 1 | $10K |
| BEAM THERAPEUTICS | Biotech/biopharmaceutical companies | Massachusetts | 1 | 1 | $10K |
Firms
Registrants who filed on the bill, by filings.
| Registrant | Clients | Filings | Reported |
|---|---|---|---|
| GRIDIRON PUBLIC AFFAIRS, LLC | 2 | 2 | $20K |
| REAL ESTATE ROUNDTABLE | 1 | 2 | — |
Lobbyists
Named on the filings that cite the bill.
| Lobbyist | Firms | Clients | Filings |
|---|---|---|---|
| CLIFTON RODGERS | 1 | 1 | 2 |
| DUANE DESIDERIO | 1 | 1 | 2 |
| GREG CHESMORE | 1 | 2 | 2 |
| JEFFREY DEBOER | 1 | 1 | 2 |
| RYAN MCCORMICK | 1 | 1 | 2 |
Filings
The documents themselves, on the Senate’s Lobbying Disclosure site, largest reported first.
| Client | Registrant | Period | Reported | Document |
|---|---|---|---|---|
| REAL ESTATE ROUNDTABLE | REAL ESTATE ROUNDTABLE | 2025 first_quarter | $1.2M | 1st Quarter - Report |
| REAL ESTATE ROUNDTABLE | REAL ESTATE ROUNDTABLE | 2025 second_quarter | $953.3K | 2nd Quarter - Report |
| BEAM THERAPEUTICS | GRIDIRON PUBLIC AFFAIRS, LLC | 2026 second_quarter | $10K | 2nd Quarter - Report |
| AGIOS PHARMACEUTICALS | GRIDIRON PUBLIC AFFAIRS, LLC | 2026 second_quarter | $10K | 2nd Quarter - Report |
Classification
The Congressional Research Service files H.R. 5187 under Armed Forces and National Security, one of its 31 policy areas.
CRS Subjects
CRS assigns every bill one policy area from its 31; H.R. 5187’s is Armed Forces and National Security.
hr5187/policy-areas.txtSource: congress.gov · legiscan.com