Both sides have signed this (Bill Ranking)
H.R. 1082 · 119th Congress (2025-2026)
2 members · Left 1 · Center 0 · Right 1 (Bill Ranking)
| Sponsor | Rep. Moolenaar, John R. (R-MI) (Introduced 02/06/2025) |
|---|---|
| Sponsor Voting Record | Lean right · DW-NOMINATE +0.45 · measured from every roll-call vote this member has cast (voteview.com) (Sponsor Ranking) |
| Support |
LLLCLRR support across the spectrum: 2 members signed on (Bill Ranking) this bill: sponsor + current cosponsors, each once |
| Committees | Senate - Health, Education, Labor, and Pensions Committee; House - Energy and Commerce Committee; House - Energy and Commerce Committee; House - Energy and Commerce Committee |
| Latest Action | 06/24/2025 Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions. |
| Roll Call Votes | There have been no roll call votes |
| Source | view on congress.gov → |
Introduced in House (02/06/2025)
Shandra Eisenga Human Cell and Tissue Product Safety Act
This bill establishes civil penalties for violations of regulations governing the donation and handling of human cell and tissue products. It also requires the Food and Drug Administration (FDA) to report on the regulation of these products and to provide related information to stakeholders. (Human cell and tissue products are articles containing or consisting of human cells or tissues that are intended for use in a human recipient.)
Specifically, the bill establishes civil penalties for violations of the FDA’s regulations on donor eligibility and current good tissue practice for manufacturing and distributing human cell and tissue products.
Also, the bill requires the FDA to conduct workshops to educate stakeholders and facilitate discussion on the science and regulation of human cell and tissue products. The FDA must establish a public docket to receive written comments on this topic, and report to Congress with recommendations. The bill also requires the FDA to support the development of educational materials for health care professionals regarding organ, tissue, and eye donations and related topics.
Additionally, the bill requires the FDA to publish on its website educational materials about the Tissue Reference Group (a working group within the FDA) and best practices for obtaining a recommendation from them about human cell and tissue products. Also, annually for three years, the FDA must publish on its website information on inquiries submitted to the Tissue Reference Group and FDA registrations and inspections regarding human cell and tissue manufacturers.
119 HR 1082 EH: Shandra Eisenga Human Cell and Tissue Product Safety Act U.S. House of Representatives text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. IB 119th CONGRESS1st Session H. R. 1082
IN THE HOUSE OF REPRESENTATIVES AN ACT To require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes.
1.Short titleThis Act may be cited as the Shandra Eisenga Human Cell and Tissue Product Safety Act.
2.DefinitionsIn this Act: (1)Human cell and tissue productThe terms human cell and tissue product and human cell and tissue products have the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations). (2)SecretaryThe term Secretary means the Secretary of Health and Human Services. (3)Tissue Reference GroupThe term Tissue Reference Group means the Tissue Reference Group of the Food and Drug Administration.
3.Human cell and tissue products transplant public awareness campaignThe Secretary shall support the development and dissemination of educational materials to inform health care professionals and other appropriate professionals about issues surrounding— (1)organ, tissue, and eye donation, including evidence-based methods to approach patients and their families; (2)the availability of any donor screening tests; and (3)other relevant aspects of donation.
4.Civil penalties for violation of requirements for human cell and tissue productsSection 368 of the Public Health Service Act (42 U.S.C. 271) is amended by adding at the end the following: (d) (1)Any person who, on or after the date of the enactment of the Shandra Eisenga Human Cell and Tissue Product Safety Act, violates a requirement of subparts C or D of section 1271 of title 21, Code of Federal Regulations, (or successor regulations) with respect to human cell or tissue products regulated under section 361 shall be liable to the United States for a civil penalty in an amount not to exceed the sum of— (A) (i)$20,000 for each violation; and (ii)in the case of a violation that continues after the Secretary provides written notice to such person, $20,000 for each subsequent day on which the violation continues; and (B)an amount equal to the retail value of the human cell and tissue products that are the subject of the violation. (2)The total civil penalty under paragraph (1) may not exceed $10,000,000 for all such violations adjudicated in a single proceeding. (3)In this subsection, the term human cell and tissue products has the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations)..
5.Streamlining regulatory oversight of human cell and tissue products (a)Information on human cell and tissue products (1)WebsiteThe Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration— (A)educational materials about the Tissue Reference Group; and (B)best practices for obtaining a timely, accurate recommendation regarding human cell and tissue products from the Tissue Reference Group. (2)Public informationNot later than 1 year after the date of the enactment of this Act, and annually for the subsequent 3 years, the Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration— (A)the number of human cell and tissue establishments that registered with the Food and Drug Administration on or after January 1, 2019; (B)the number of inspections conducted by the Food and Drug Administration of human cell and tissue establishments on or after January 1, 2019, including a comparison of the number of inspections for blood establishments with the number of inspections for such human cell and tissue establishments; (C)the number and type of inquiries to the Tissue Reference Group in the preceding year; and (D)the average response time for submissions to the Tissue Reference Group in the preceding year, including average initial and final response time. (3)EducationThe Secretary, acting through the Commissioner of Food and Drugs, shall, with respect to the regulation of human cell and tissue products— (A)provide information to relevant stakeholders, including industry, tissue establishments, academic health centers, biomedical consortia, research organizations, and patients; and (B)conduct workshops and other interactive and educational sessions for such stakeholders to help support regulatory predictability and scientific advancement, as appropriate. (b)Human cell and tissue product scientific and regulatory updatesSection 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) is amended by striking best practices and all that follows through other cellular therapies and inserting best practices on generating scientific data necessary to further facilitate the development of certain human cell-, tissue-, and cellular-based medical products (and the latest scientific information about such products), namely, stem cell and other cellular therapies. (c)Public docketNot later than 60 days after the date of the enactment of this Act, the Secretary shall establish a public docket to receive written comments related to— (1)the approaches recommended for discussion during the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328); and (2)modernizing the regulation of human cell and tissue products, including considerations associated with assessing minimal manipulation and homologous use (as such terms are defined in section 1271.3 of title 21, Code of Federal Regulations (or successor regulations)) of human cell and tissue products. (d)Report to CongressNot later than September 30, 2026, the Secretary shall summarize the approaches discussed in the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) and the public docket described in subsection (c), and develop recommendations regarding the regulation of human cell and tissue products, including provisions under sections 1271.10(a) and 1271.3 of title 21, Code of Federal Regulations, taking into account— (1)regulatory burden; (2)scientific developments; (3)access to human cell and tissue products regulated under section 361 of the Public Health Service Act (42 U.S.C. 264); and (4)protecting public health. Passed the House of Representatives June 23, 2025.Kevin F. McCumber,Clerk.
117 HR 1082 IH: Shandra Eisenga Human Cell and Tissue Product Safety Act U.S. House of Representatives 2025-02-06 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. I119th CONGRESS1st SessionH. R. 1082IN THE HOUSE OF REPRESENTATIVESFebruary 6, 2025Mr. Moolenaar (for himself and Mrs. Dingell) introduced the following bill; which was referred to the Committee on Energy and CommerceA BILLTo require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes.1.Short titleThis Act may be cited as the Shandra Eisenga Human Cell and Tissue Product Safety Act.2.DefinitionsIn this Act:(1)Human cell and tissue productThe terms human cell and tissue product and human cell and tissue products have the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations).(2)SecretaryThe term Secretary means the Secretary of Health and Human Services.(3)Tissue Reference GroupThe term Tissue Reference Group means the Tissue Reference Group of the Food and Drug Administration.3.Human cell and tissue products transplant public awareness campaignThe Secretary shall support the development and dissemination of educational materials to inform health care professionals and other appropriate professionals about issues surrounding—(1)organ, tissue, and eye donation, including evidence-based methods to approach patients and their families;(2)the availability of any donor screening tests; and(3)other relevant aspects of donation.4.Civil penalties for violation of requirements for human cell and tissue productsSection 368 of the Public Health Service Act (42 U.S.C. 271) is amended by adding at the end the following:(d)(1)Any person who, on or after the date of the enactment of the Shandra Eisenga Human Cell and Tissue Product Safety Act, violates a requirement of subparts C or D of section 1271 of title 21, Code of Federal Regulations, (or successor regulations) with respect to human cell or tissue products regulated under section 361 shall be liable to the United States for a civil penalty in an amount not to exceed the sum of—(A)(i)$20,000 for each violation; and(ii)in the case of a violation that continues after the Secretary provides written notice to such person, $20,000 for each subsequent day on which the violation continues; and(B)an amount equal to the retail value of the human cell and tissue products that are the subject of the violation.(2)The total civil penalty under paragraph (1) may not exceed $10,000,000 for all such violations adjudicated in a single proceeding.(3)In this subsection, the term human cell and tissue products has the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations)..5.Streamlining regulatory oversight of human cell and tissue products(a)Information on human cell and tissue products(1)WebsiteThe Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)educational materials about the Tissue Reference Group; and(B)best practices for obtaining a timely, accurate recommendation regarding human cell and tissue products from the Tissue Reference Group.(2)Public informationNot later than 1 year after the date of the enactment of this Act, and annually for the subsequent 3 years, the Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)the number of human cell and tissue establishments that registered with the Food and Drug Administration on or after January 1, 2019;(B)the number of inspections conducted by the Food and Drug Administration of human cell and tissue establishments on or after January 1, 2019, including a comparison of the number of inspections for blood establishments with the number of inspections for such human cell and tissue establishments;(C)the number and type of inquiries to the Tissue Reference Group in the preceding year; and(D)the average response time for submissions to the Tissue Reference Group in the preceding year, including average initial and final response time.(3)EducationThe Secretary, acting through the Commissioner of Food and Drugs, shall, with respect to the regulation of human cell and tissue products—(A)provide information to relevant stakeholders, including industry, tissue establishments, academic health centers, biomedical consortia, research organizations, and patients; and(B)conduct workshops and other interactive and educational sessions for such stakeholders to help support regulatory predictability and scientific advancement, as appropriate.(b)Human cell and tissue product scientific and regulatory updatesSection 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) is amended by striking best practices and all that follows through other cellular therapies and inserting best practices on generating scientific data necessary to further facilitate the development of certain human cell-, tissue-, and cellular-based medical products (and the latest scientific information about such products), namely, stem cell and other cellular therapies.(c)Public docketNot later than 60 days after the date of the enactment of this Act, the Secretary shall establish a public docket to receive written comments related to—(1)the approaches recommended for discussion during the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328); and(2)modernizing the regulation of human cell and tissue products, including considerations associated with assessing minimal manipulation and homologous use (as such terms are defined in section 1271.3 of title 21, Code of Federal Regulations (or successor regulations)) of human cell and tissue products.(d)Report to CongressNot later than September 30, 2026, the Secretary shall summarize the approaches discussed in the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) and the public docket described in subsection (c), and develop recommendations regarding the regulation of human cell and tissue products, including provisions under sections 1271.10(a) and 1271.3 of title 21, Code of Federal Regulations, taking into account—(1)regulatory burden;(2)scientific developments;(3)access to human cell and tissue products regulated under section 361 of the Public Health Service Act (42 U.S.C. 264); and(4)protecting public health.
117 HR 1082 : Shandra Eisenga Human Cell and Tissue Product Safety Act U.S. House of Representatives text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. IIB119th CONGRESS1st SessionH. R. 1082IN THE SENATE OF THE UNITED STATESJune 24, 2025Received; read twice and referred to the Committee on Health, Education, Labor, and PensionsAN ACTTo require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes.1.Short titleThis Act may be cited as the Shandra Eisenga Human Cell and Tissue Product Safety Act.2.DefinitionsIn this Act:(1)Human cell and tissue productThe terms human cell and tissue product and human cell and tissue products have the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations).(2)SecretaryThe term Secretary means the Secretary of Health and Human Services.(3)Tissue Reference GroupThe term Tissue Reference Group means the Tissue Reference Group of the Food and Drug Administration.3.Human cell and tissue products transplant public awareness campaignThe Secretary shall support the development and dissemination of educational materials to inform health care professionals and other appropriate professionals about issues surrounding—(1)organ, tissue, and eye donation, including evidence-based methods to approach patients and their families;(2)the availability of any donor screening tests; and(3)other relevant aspects of donation.4.Civil penalties for violation of requirements for human cell and tissue productsSection 368 of the Public Health Service Act (42 U.S.C. 271) is amended by adding at the end the following:(d)(1)Any person who, on or after the date of the enactment of the Shandra Eisenga Human Cell and Tissue Product Safety Act, violates a requirement of subparts C or D of section 1271 of title 21, Code of Federal Regulations, (or successor regulations) with respect to human cell or tissue products regulated under section 361 shall be liable to the United States for a civil penalty in an amount not to exceed the sum of—(A)(i)$20,000 for each violation; and(ii)in the case of a violation that continues after the Secretary provides written notice to such person, $20,000 for each subsequent day on which the violation continues; and(B)an amount equal to the retail value of the human cell and tissue products that are the subject of the violation.(2)The total civil penalty under paragraph (1) may not exceed $10,000,000 for all such violations adjudicated in a single proceeding.(3)In this subsection, the term human cell and tissue products has the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations)..5.Streamlining regulatory oversight of human cell and tissue products(a)Information on human cell and tissue products(1)WebsiteThe Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)educational materials about the Tissue Reference Group; and(B)best practices for obtaining a timely, accurate recommendation regarding human cell and tissue products from the Tissue Reference Group.(2)Public informationNot later than 1 year after the date of the enactment of this Act, and annually for the subsequent 3 years, the Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)the number of human cell and tissue establishments that registered with the Food and Drug Administration on or after January 1, 2019;(B)the number of inspections conducted by the Food and Drug Administration of human cell and tissue establishments on or after January 1, 2019, including a comparison of the number of inspections for blood establishments with the number of inspections for such human cell and tissue establishments;(C)the number and type of inquiries to the Tissue Reference Group in the preceding year; and(D)the average response time for submissions to the Tissue Reference Group in the preceding year, including average initial and final response time.(3)EducationThe Secretary, acting through the Commissioner of Food and Drugs, shall, with respect to the regulation of human cell and tissue products—(A)provide information to relevant stakeholders, including industry, tissue establishments, academic health centers, biomedical consortia, research organizations, and patients; and(B)conduct workshops and other interactive and educational sessions for such stakeholders to help support regulatory predictability and scientific advancement, as appropriate.(b)Human cell and tissue product scientific and regulatory updatesSection 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) is amended by striking best practices and all that follows through other cellular therapies and inserting best practices on generating scientific data necessary to further facilitate the development of certain human cell-, tissue-, and cellular-based medical products (and the latest scientific information about such products), namely, stem cell and other cellular therapies.(c)Public docketNot later than 60 days after the date of the enactment of this Act, the Secretary shall establish a public docket to receive written comments related to—(1)the approaches recommended for discussion during the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328); and(2)modernizing the regulation of human cell and tissue products, including considerations associated with assessing minimal manipulation and homologous use (as such terms are defined in section 1271.3 of title 21, Code of Federal Regulations (or successor regulations)) of human cell and tissue products.(d)Report to CongressNot later than September 30, 2026, the Secretary shall summarize the approaches discussed in the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) and the public docket described in subsection (c), and develop recommendations regarding the regulation of human cell and tissue products, including provisions under sections 1271.10(a) and 1271.3 of title 21, Code of Federal Regulations, taking into account—(1)regulatory burden;(2)scientific developments;(3)access to human cell and tissue products regulated under section 361 of the Public Health Service Act (42 U.S.C. 264); and(4)protecting public health.Passed the House of Representatives June 23, 2025.Kevin F. McCumber,Clerk.
117 HR 1082 RH: Shandra Eisenga Human Cell and Tissue Product Safety Act U.S. House of Representatives 2025-06-12 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. IBUnion Calendar No. 127119th CONGRESS1st SessionH. R. 1082[Report No. 119–160]IN THE HOUSE OF REPRESENTATIVESFebruary 6, 2025Mr. Moolenaar (for himself and Mrs. Dingell) introduced the following bill; which was referred to the Committee on Energy and CommerceJune 12, 2025Committed to the Committee of the Whole House on the State of the Union and ordered to be printedA BILLTo require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes.1.Short titleThis Act may be cited as the Shandra Eisenga Human Cell and Tissue Product Safety Act.2.DefinitionsIn this Act:(1)Human cell and tissue productThe terms human cell and tissue product and human cell and tissue products have the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations).(2)SecretaryThe term Secretary means the Secretary of Health and Human Services.(3)Tissue Reference GroupThe term Tissue Reference Group means the Tissue Reference Group of the Food and Drug Administration.3.Human cell and tissue products transplant public awareness campaignThe Secretary shall support the development and dissemination of educational materials to inform health care professionals and other appropriate professionals about issues surrounding—(1)organ, tissue, and eye donation, including evidence-based methods to approach patients and their families;(2)the availability of any donor screening tests; and(3)other relevant aspects of donation.4.Civil penalties for violation of requirements for human cell and tissue productsSection 368 of the Public Health Service Act (42 U.S.C. 271) is amended by adding at the end the following:(d)(1)Any person who, on or after the date of the enactment of the Shandra Eisenga Human Cell and Tissue Product Safety Act, violates a requirement of subparts C or D of section 1271 of title 21, Code of Federal Regulations, (or successor regulations) with respect to human cell or tissue products regulated under section 361 shall be liable to the United States for a civil penalty in an amount not to exceed the sum of—(A)(i)$20,000 for each violation; and(ii)in the case of a violation that continues after the Secretary provides written notice to such person, $20,000 for each subsequent day on which the violation continues; and(B)an amount equal to the retail value of the human cell and tissue products that are the subject of the violation.(2)The total civil penalty under paragraph (1) may not exceed $10,000,000 for all such violations adjudicated in a single proceeding.(3)In this subsection, the term human cell and tissue products has the meaning given the term human cells, tissues, or cellular or tissue-based products in section 1271.3(d) of title 21, Code of Federal Regulations (or successor regulations)..5.Streamlining regulatory oversight of human cell and tissue products(a)Information on human cell and tissue products(1)WebsiteThe Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)educational materials about the Tissue Reference Group; and(B)best practices for obtaining a timely, accurate recommendation regarding human cell and tissue products from the Tissue Reference Group.(2)Public informationNot later than 1 year after the date of the enactment of this Act, and annually for the subsequent 3 years, the Secretary, acting through the Commissioner of Food and Drugs, shall publish on the public website of the Food and Drug Administration—(A)the number of human cell and tissue establishments that registered with the Food and Drug Administration on or after January 1, 2019;(B)the number of inspections conducted by the Food and Drug Administration of human cell and tissue establishments on or after January 1, 2019, including a comparison of the number of inspections for blood establishments with the number of inspections for such human cell and tissue establishments;(C)the number and type of inquiries to the Tissue Reference Group in the preceding year; and(D)the average response time for submissions to the Tissue Reference Group in the preceding year, including average initial and final response time.(3)EducationThe Secretary, acting through the Commissioner of Food and Drugs, shall, with respect to the regulation of human cell and tissue products—(A)provide information to relevant stakeholders, including industry, tissue establishments, academic health centers, biomedical consortia, research organizations, and patients; and(B)conduct workshops and other interactive and educational sessions for such stakeholders to help support regulatory predictability and scientific advancement, as appropriate.(b)Human cell and tissue product scientific and regulatory updatesSection 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) is amended by striking best practices and all that follows through other cellular therapies and inserting best practices on generating scientific data necessary to further facilitate the development of certain human cell-, tissue-, and cellular-based medical products (and the latest scientific information about such products), namely, stem cell and other cellular therapies.(c)Public docketNot later than 60 days after the date of the enactment of this Act, the Secretary shall establish a public docket to receive written comments related to—(1)the approaches recommended for discussion during the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328); and(2)modernizing the regulation of human cell and tissue products, including considerations associated with assessing minimal manipulation and homologous use (as such terms are defined in section 1271.3 of title 21, Code of Federal Regulations (or successor regulations)) of human cell and tissue products.(d)Report to CongressNot later than September 30, 2026, the Secretary shall summarize the approaches discussed in the public workshop described in section 3205 of the Food and Drug Omnibus Reform Act of 2022 (title III of division FF of Public Law 117–328) and the public docket described in subsection (c), and develop recommendations regarding the regulation of human cell and tissue products, including provisions under sections 1271.10(a) and 1271.3 of title 21, Code of Federal Regulations, taking into account—(1)regulatory burden;(2)scientific developments;(3)access to human cell and tissue products regulated under section 361 of the Public Health Service Act (42 U.S.C. 264); and(4)protecting public health.June 12, 2025Committed to the Committee of the Whole House on the State of the Union and ordered to be printed
The bill's own words, from our database (synced from the GPO BILLS XML); paragraph breaks added at the bill's section boundaries, nothing else changed.
| Date | Chamber | All Actions |
|---|---|---|
| 02/06/2025 | Library of Congress | Introduced in House |
| 02/06/2025 | Library of Congress | Introduced in House |
| 02/06/2025 | House floor actions | Referred to the House Committee on Energy and Commerce. |
| 04/29/2025 | House committee actions | Committee Consideration and Mark-up Session Held |
| 04/29/2025 | House committee actions | Ordered to be Reported by Voice Vote. |
| 06/12/2025 | Library of Congress | Reported by the Committee on Energy and Commerce. H. Rept. 119-160. |
| 06/12/2025 | House floor actions | Reported by the Committee on Energy and Commerce. H. Rept. 119-160. |
| 06/12/2025 | House floor actions | Placed on the Union Calendar, Calendar No. 127. |
| 06/23/2025 | House floor actions | Mr. Bilirakis moved to suspend the rules and pass the bill. |
| 06/23/2025 | House floor actions | Considered under suspension of the rules. (consideration: CR H2860-2862) |
| 06/23/2025 | House floor actions | DEBATE - The House proceeded with forty minutes of debate on H.R. 1082. |
| 06/23/2025 | Library of Congress | Passed/agreed to in House: On motion to suspend the rules and pass the bill Agreed to by voice vote. (text: CR H2860-2861) |
| 06/23/2025 | House floor actions | On motion to suspend the rules and pass the bill Agreed to by voice vote. (text: CR H2860-2861) |
| 06/23/2025 | House floor actions | Motion to reconsider laid on the table Agreed to without objection. |
| 06/24/2025 | Senate | Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions. |
| Title Type | Title |
|---|---|
| Official Titles from EH (Engrossed in House) bill text | To require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes. |
| Short Titles from RFS (Referred to Senate) bill text | Shandra Eisenga Human Cell and Tissue Product Safety Act |
| Short Title(s) as Passed House | Shandra Eisenga Human Cell and Tissue Product Safety Act |
| Short Title(s) as Reported to House | Shandra Eisenga Human Cell and Tissue Product Safety Act |
| Display Title | Shandra Eisenga Human Cell and Tissue Product Safety Act |
| Short Title(s) as Introduced | Shandra Eisenga Human Cell and Tissue Product Safety Act |
| Official Title as Introduced | To require the Secretary of Health and Human Services to conduct a national, evidence-based education campaign to increase public and health care provider awareness regarding the potential risks and benefits of human cell and tissue products transplants, and for other purposes. |
There are no amendments to this bill.
* = Original cosponsor
| Committee | Activity |
|---|---|
| Senate - Health, Education, Labor, and Pensions Committee | 06/24/2025 Referred To |
| House - Energy and Commerce Committee | 06/12/2025 Reported By |
| House - Energy and Commerce Committee | 04/29/2025 Markup By |
| House - Energy and Commerce Committee | 02/06/2025 Referred To |
Policy Area: Health
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