HR 1862 · 112th Congress 2011–2013, ended

Regenerative Medicine Promotion Act of 2011

Fact sheet

Latest action · May 13, 2011 Referred to the Subcommittee on Health.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedMay 12, 2011
  2. Passed HouseNot reached
  3. Passed SenateNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

Regenerative Medicine Promotion Act of 2011 - Requires the Comptroller General to submit to Congress a report identifying all ongoing federal programs and activities regarding regenerative medicine.

Directs the Secretary of Health and Human Services (HHS) to establish a Regenerative Medicine Coordinating Council in the Office of the Secretary, the duties of which shall include: (1) preparing a national strategy to support research into regenerative medicine and the development of drugs, biological products, medical devices, and biomaterials for use in regenerative medicine; (2) identifying sources of funding for research into regenerative medicine and areas where such funding is inadequate; and (3) making recommendations regarding federal policies to support development and marketing of regenerative medicine products.

Authorizes the Secretary, acting through the Director of the National Institutes of Health (NIH), to make grants for: (1) basic or preclinical research into regenerative medicine; (2) research and development of drugs, biological products, medical devices, and biomaterials for use in regenerative medicine; and (3) the making of an investigational new drug application or an investigational device exemption application within four years of receiving such grant.

Amends the Public Health Service Act to authorize the Director of NIH to award grants, contracts, or cooperative agreements to accelerate the development of high need cures through the development of medical products and behavioral therapies for use in regenerative medicine.

Authorizes the Secretary, acting through the Commissioner of Food and Drugs, to: (1) conduct, support, or collaborate in regulatory research to assist the Food and Drug Administration (FDA) in performing its functions with respect to regenerative medicine; or (2) make grants to fund regulatory research for such purpose.

Cosponsors 19

Members who signed on, in the order they did. Signatures ran from May 12, 2011 to Nov 13, 2012, with 7 there on the day it was introduced.

SeatCosponsorSigned on
R-PACharles W. DentOriginalMay 12, 2011
D-CODiana DeGetteOriginalMay 12, 2011
D-NCG. K. ButterfieldOriginalMay 12, 2011
D-RIJames R. LangevinOriginalMay 12, 2011
R-PAJim GerlachOriginalMay 12, 2011
D-OHMarcia L. FudgeOriginalMay 12, 2011
D-NJRush HoltOriginalMay 12, 2011
D-CAAnna G. EshooJun 2, 2011
D-MAMichael E. CapuanoJun 21, 2011
R-OHSteven C. LaTouretteJun 21, 2011
D-CASam FarrSep 21, 2011
D-MABarney FrankOct 6, 2011
D-MAJames P. McGovernOct 6, 2011
D-ILJesse L. Jackson, Jr.Oct 6, 2011
R-TXMichael C. BurgessDec 14, 2011

Actions 3

Everything that happened, newest first.

  1. May 13, 2011Referred to the Subcommittee on Health.
  2. May 12, 2011Introduced in House
  3. May 12, 2011Referred to the House Committee on Energy and Commerce.

Subjects

Assigned by the Library of Congress. Policy area: Health.

Text 1

Each version as it was printed, newest first.

  1. May 12, 2011Introduced in House

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov.