H.R. 7881 (93rd): Hemophilia Act

Introduced:
May 16, 1973 (93rd Congress, 1973–1974)
Status:
Died (Referred to Committee)
See Instead:

H.R. 11806 (same title)
Referred to Committee — Dec 05, 1973

H.R. 11761 (same title)
Referred to Committee — Dec 04, 1973

H.R. 11591 (same title)
Referred to Committee — Nov 27, 1973

H.R. 11219 (same title)
Referred to Committee — Oct 31, 1973

H.R. 10423 (same title)
Referred to Committee — Sep 20, 1973

H.R. 9340 (same title)
Referred to Committee — Jul 17, 1973

H.R. 8143 (same title)
Referred to Committee — May 24, 1973

Sponsor
Richard Hanna
Representative for California's 34th congressional district
Party
Democrat
Related Bills
H.R. 11806 (identical)

Referred to Committee
Last Action: Dec 05, 1973

H.R. 11761 (identical)

Referred to Committee
Last Action: Dec 04, 1973

 
Status

This bill was introduced on May 16, 1973, in a previous session of Congress, but was not enacted.

Progress
Introduced May 16, 1973
Referred to Committee May 16, 1973
 
Full Title

A bill to amend the Public Health Service Act to provide for programs for the diagnosis and treatment of hemophilia.

Summary

No summaries available.

Cosponsors
none
Committees

House Energy and Commerce

The committee chair determines whether a bill will move past the committee stage.

 
Primary Source

THOMAS.gov (The Library of Congress)

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Notes

H.R. stands for House of Representatives bill.

A bill must be passed by both the House and Senate in identical form and then be signed by the president to become law.

The bill’s title was written by its sponsor.

GovTrack’s Bill Summary

We don’t have a summary available yet.

Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


5/16/1973--Introduced.
Hemophilia Act - Provides that any individual suffering from hemophilia may file a claim for benefits under this part with the Secretary of Health, Education and Welfare in such form and containing such information as he may reasonably require.
States that benefits under this part shall be paid to, or on behalf of a claimant, in an amount equal to 100 percent of the actual cost of providing blood, blood products, and services associated with the treatment of hemophilia, less:
(1) amounts payable by third parties (including governmental agencies), and
(2) amounts determined by the Secretary (in accordance with this Act) to be payable by the individual suffering from hemophilia.
Authorizes to be appropriated for the fiscal years beginning July 1, 1973, and ending June 30, 1976, such sums as may be necessary to carry out the purpose of this Act. Directs the Secretary to provide for the establishment of no less than fifteen new centers for the diagnosis and treatment of individuals suffering from hempophilia.
Authorizes to be appropriated to carry out the purposes of this section $5,000,000 for the fiscal year ending June 30, 1974, $10,000,000 for the fiscal year ending June 30, 1975, and $15,000,000 for the fiscal year ending June 30, 1976.
Provides the Secretary shall establish a program within the Public Health Service to provide for diagnosis, treatment, and counseling of individuals suffering from hemophilia.
States that such program shall be made available through the facilities of the Public Health Service to any individual requesting diagnosis, treatment, or counseling for hemophilia.
Permits the Secretary to make grants to public and nonprofit private entities, and to enter into contracts with public and private entities and individuals to establish blood fractionation centers, for the purpose of fractionating and making available for distribution blood and blood products, in accordance with regulations prescribed by the Secretary to hemophilia treatment and diagnostic centers.
Authorizes to be appropriated $5,000,000 for the fiscal year ending June 30, 1974, $10,000,000 for the fiscal year ending June 30, 1975, and $15,000,000 for the fiscal year ending June 30, 1976 for this purpose.
Establishes in the National Institutes of Health a National Hemophilia Advisory Board to be composed of twenty members.
States that it shall be the function of the Board to:
(1) establish guidelines for the diagnosis and treatment of persons suffering from hemophilia; and
(2) submit a report to the President for transmittal to the Congress not later than January 31 of each year on the scope of actions conducted under this Act.

House Republican Conference Summary

The summary below was written by the House Republican Conference, which is the caucus of Republicans in the House of Representatives.


No summary available.

House Democratic Caucus Summary

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