Federal
To provide for quality assurance of COVID-19 reimbursements and reporting.
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I
116TH CONGRESS
2D SESSION
H. R. 7037
To provide for quality assurance of COVID–19 reimbursements and reporting.
IN THE HOUSE OF REPRESENTATIVES
MAY 27, 2020
Mr. POSEY introduced the following bill; which was referred to the Committee
on Energy and Commerce, and in addition to the Committee on the Judi-
ciary, 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
A BILL
To provide for quality assurance of COVID–19
reimbursements and reporting.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. QUALITY ASSURANCE OF COVID–19 REIM-
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BURSEMENTS AND REPORTING.
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(a) IN GENERAL.—Notwithstanding any other provi-
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sion of law, no Federal funds shall be used for a reim-
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bursement or payment for—
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(1) COVID–19 testing of any individual unless
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the request for such reimbursement or payment is
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•HR 7037 IH
accompanied by evidence that the individual was
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tested using a test that was approved, cleared, or
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authorized under section 510(k), 513, 515, or 564
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of the Federal Food, Drug, and Cosmetic Act (21
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U.S.C. 360(k), 360c, 360e, 360bbb–3) for COVID–
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19 diagnosis; or
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(2) COVID–19 treatment of any individual un-
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less the request for reimbursement or payment is ac-
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companied by evidence that the person tested posi-
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tive for COVID–19 using a test that was approved,
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cleared, or authorized under section 510(k), 513,
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515, or 564 of the Federal Food, Drug, and Cos-
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metic Act (21 U.S.C. 360(k), 360c, 360e, 360bbb–
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3) for COVID–19 diagnosis.
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(b) QUALITY ASSURANCE OF REIMBURSEMENTS.—
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For purposes of subsection (a), notwithstanding any other
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provision of law, the head of any Federal agency author-
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ized to make a reimbursement or payment for COVID–
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19 testing or treatment of individuals shall review each
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request presented for such reimbursement or payment
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and—
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(1) deny any request for such a reimbursement
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or payment for COVID–19 testing of an individual
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or, if reimbursement or payment has already been
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made, cause to be recovered such reimbursement or
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payment, unless the request is accompanied by evi-
1
dence that the individual was tested using a test
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that was approved, cleared, or authorized under sec-
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tion 510(k), 513, 515, or 564 of the Federal Food,
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Drug, and Cosmetic Act (21 U.S.C. 360(k), 360c,
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360e, 360bbb–3) for COVID–19 diagnosis as of the
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date of the review of the head of the agency;
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(2) deny any request for such a reimbursement
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or payment for COVID–19 treatment of an indi-
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vidual or, if reimbursement or payment has already
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been made, cause to be recovered such reimburse-
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ment or payment, unless the request is accompanied
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by evidence that the individual tested positive for
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COVID–19 using a test that was approved, cleared,
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or authorized under section 510(k), 513, 515, or
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564 of the Federal Food, Drug, and Cosmetic Act
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(21 U.S.C. 360(k), 360c, 360e, 360bbb–3) for
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COVID–19 diagnosis as of the date of the review of
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the head of the agency; and
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(3) provide to the Director of the Centers for
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Disease Control and Prevention the results of such
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review.
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(c) CORRECTION OF REPORTS.—The Director of the
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Centers for Disease Control and Prevention shall apply
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the results provided to the Director under subsection
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(b)(3) to—
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(1) exclude from the official United States
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count of cases of COVID–19 any individual reported
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to have been positive for COVID–19 in a request
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subject to review in subsection (b) but where the
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agency head involved found the request was not ac-
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companied by evidence that the individual had been
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tested positive for COVID–19 using a test that was
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approved, cleared, or authorized under section
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510(k), 513, 515, or 564 of the Federal Food,
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Drug, and Cosmetic Act (21 U.S.C. 360(k), 360c,
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360e, 360bbb–3) for diagnosis of COVID–19; and
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(2) exclude from the official United States
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count of deaths due to COVID–19 any individual
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who died and was reported to have been treated or
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tested positive for COVID–19 in a request subject to
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review under subsection (b) but where the agency
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head involved found the request was not accom-
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panied by evidence that the individual had been test-
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ed positive for COVID–19 using a test that was ap-
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proved, cleared, or authorized under section 510(k),
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513, 515, or 564 of the Federal Food, Drug, and
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Cosmetic Act (21 U.S.C. 360(k), 360c, 360e,
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360bbb–3) for diagnosis of COVID–19.
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(d) PENALTY.—Any person who knowingly reports a
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false diagnosis of COVID–19 shall be imprisoned not more
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than 10 years and fined under title 18, United States
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Code, or both.
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Æ
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