[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 6238 Introduced in House (IH)]
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116th CONGRESS
2d Session
H. R. 6238
To amend the Internal Revenue Code of 1986 to restore the amount of the
orphan drug tax credit, and for other purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
March 12, 2020
Mr. Gottheimer (for himself and Mr. Upton) introduced the following
bill; which was referred to the Committee on Ways and Means, and in
addition to the Committee on Energy and Commerce, for a period to be
subsequently determined by the Speaker, in each case for consideration
of such provisions as fall within the jurisdiction of the committee
concerned
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A BILL
To amend the Internal Revenue Code of 1986 to restore the amount of the
orphan drug tax credit, and for other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as ``Cameron's Law''.
SEC. 2. RESTORATION OF AMOUNT OF ORPHAN DRUG TAX CREDIT.
(a) In General.--Section 45C(a) of the Internal Revenue Code of
1986 is amended by striking ``25 percent'' and inserting ``50
percent''.
(b) Effective Date.--The amendment made by this section shall apply
to taxable years beginning after the date of the enactment of this Act.
SEC. 3. CDC STUDY ON SURVEILLANCE INFRASTRUCTURE FOR RARE DISEASES AND
CONDITIONS.
(a) Study.--Not later than 1 year after the date of enactment of
this Act, the Director of the Centers for Disease Control and
Prevention (in this section referred to as the ``Director'') shall
complete a study on enhancing and expanding the infrastructure to track
the epidemiology of rare diseases and conditions, including with
respect to the following:
(1) Rates of mortality.
(2) Potential for research and treatment.
(3) Demographics.
(4) Diagnosis and progression markers.
(5) The history of the disease or condition.
(6) Detection management.
(b) Consultation.--In conducting the study required by subsection
(a), the Director shall consult with relevant experts, including--
(1) epidemiologists with experience in disease
surveillance;
(2) representatives of national voluntary health
associations;
(3) health information technology experts or other
information management specialists;
(4) clinicians with expertise in rare diseases or
conditions;
(5) research scientists with expertise in rare diseases or
conditions, or experience conducting translational research or
utilizing surveillance systems for scientific research
purposes; and
(6) patients, and caregivers of patients, with rare
diseases or conditions.
(c) Report.--Not later than 3 months after completing the study
required by subsection (a), the Director shall submit a report to the
Congress on the results of the study.
(d) Definition.--In this section, the terms ``rare diseases and
conditions'' and ``rare diseases or conditions'' refer to human
diseases and conditions that are--
(1) a rare disease or condition, as defined in section 526
of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360bb);
or
(2) determined by the Director to be rare and lacking in
treatment options, so as to warrant consideration in the study
required by subsection (a).
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