Monitoring and Obtaining Needed Information to Track Opioids Responsibly Act of 2017 or the MONITOR Act of 2017
This bill amends the 21st Century Cures Act to require that in order for a state to receive funds to address the opioid abuse crisis the state's prescription drug monitoring program must meet specified requirements, including reporting within one business day when controlled substances are dispensed.
[Congressional Bills 115th Congress]
[From the U.S. Government Publishing Office]
[H.R. 4236 Introduced in House (IH)]
<DOC>
115th CONGRESS
1st Session
H. R. 4236
To ensure that the prescription drug monitoring program of each State
receiving funds through the Account for the State Response to the
Opioid Abuse Crisis meets certain minimum requirements, and for other
purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
November 3, 2017
Mr. Fitzpatrick (for himself, Ms. Kuster of New Hampshire, Mr.
MacArthur, and Mr. Norcross) introduced the following bill; which was
referred to the Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To ensure that the prescription drug monitoring program of each State
receiving funds through the Account for the State Response to the
Opioid Abuse Crisis meets certain minimum requirements, 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 the ``Monitoring and Obtaining Needed
Information to Track Opioids Responsibly Act of 2017'' or the ``MONITOR
Act of 2017''.
SEC. 2. MINIMUM REQUIREMENTS FOR STATE PRESCRIPTION DRUG MONITORING
PROGRAMS.
Section 1003 of the 21st Century Cures Act (42 U.S.C. 290ee-3 note;
relating to the Account for the State Response to the Opioid Abuse
Crisis) is amended--
(1) by redesignating subsection (f) as subsection (g); and
(2) by inserting after subsection (e) the following:
``(f) Minimum Requirements for State Prescription Drug Monitoring
Programs.--
``(1) In general.--As a condition on receipt of a grant
under this section, a State shall--
``(A) certify that the State has in effect a
prescription drug monitoring program meeting the
requirements of paragraph (2); or
``(B) agree to use a portion of the funds received
through the grant to meet (or make progress in meeting)
the requirements of paragraph (2).
``(2) Requirements.--To meet the requirements of this
paragraph, a State's prescription drug monitoring program must
meet each of the following:
``(A) The program complies with the uniform
electronic format specified by the Secretary under
paragraph (3) for the reporting, sharing, and
disclosure of information.
``(B) The program meets the standards of
interoperability specified by the Secretary under
paragraph (3).
``(C) The State requires dispensers to report to
the program each dispensing in the State of a
controlled substance listed in schedule II, III, or IV
of section 202(c) of the Controlled Substances Act (21
U.S.C. 812(c)) no later than 1 business day after the
controlled substance is dispensed to the patient.
``(D) The program makes reported information
available to practitioners on a timely basis.
``(3) Uniform electronic format; interoperability.--
``(A) Establishment.--Not later than one year after
the date of enactment of this Act, the Secretary shall
specify for prescription drug monitoring programs--
``(i) a uniform electronic format for the
reporting, sharing, and disclosure of
information; and
``(ii) standards of interoperability.
``(B) Advisory group.--In carrying out subparagraph
(A), the Secretary shall--
``(i) convene an advisory group of licensed
and practicing community pharmacists and other
health practitioners who prescribe and
dispense; and
``(ii) take the recommendations of such
advisory group into consideration.
``(4) Definitions.--In this subsection:
``(A) The term `controlled substance' has the
meaning given to that term in section 102 of the
Controlled Substances Act (21 U.S.C. 802).
``(B) The term `dispenser' means a person licensed
or otherwise authorized by a State to deliver a
prescription drug product to a patient or an agent of
the patient.
``(C) The term `practitioner' means a practitioner
registered under section 303(f) of the Controlled
Substances Act (21 U.S.C. 823(f)) to prescribe,
administer, or dispense controlled substances.
``(D) The term `State' means each of the several
States and the District of Columbia.''.
<all>
Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
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