[Congressional Bills 118th Congress]
[From the U.S. Government Publishing Office]
[H.R. 4692 Introduced in House (IH)]
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118th CONGRESS
1st Session
H. R. 4692
To amend the Federal Food, Drug, and Cosmetic Act to prevent the use of
patents, trade secrets, or other intellectual property to inhibit
competition.
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IN THE HOUSE OF REPRESENTATIVES
July 17, 2023
Ms. Slotkin introduced the following bill; which was referred to the
Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To amend the Federal Food, Drug, and Cosmetic Act to prevent the use of
patents, trade secrets, or other intellectual property to inhibit
competition.
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 ``Increasing Prescription Drug
Competition Act''.
SEC. 2. PREVENTING THE USE OF PATENTS, TRADE SECRETS, OR OTHER
INTELLECTUAL PROPERTY ON RISK EVALUATION AND MITIGATION
STRATEGIES TO INHIBIT COMPETITION.
Section 505-1 of the Federal Food, Drug, and Cosmetic Act (21
U.S.C. 355-1) is amended by adding at the end the following:
``(n) Additional Requirements.--
``(1) Patents claiming rems.--If an application under
subsection (b)(2) or (j) of section 505 includes a
certification under subsection (b)(2)(A) or (j)(2)(A)(vii) of
section 505 with respect to a patent that claims an aspect of
the elements to assure safe use of a risk evaluation and
mitigation strategy requirements under subsection (f) for the
applicable listed drug, such certification shall have no effect
on the effective date of the approval of the application,
notwithstanding subparagraphs (B) and (C) of section 505(c)(3)
and clauses (ii) and (iii) of section 505(j)(5)(B).
``(2) Damages.--In the event that the sponsor of another
application under section 505 of this Act or section 351 of the
Public Health Service Act infringes a patent, trade secret, or
any other intellectual property held by the sponsor or holder
to comply with risk evaluation and mitigation strategy
requirements under this section, the sponsor or holder of the
approved application shall not seek, or claim entitlement to,
any remedy other than damages arising from the infringement.
``(3) Clarifications.--Nothing in this section shall be
construed as--
``(A) prohibiting the sponsor or holder of an
approved application from allowing the sponsor of
another application under section 505 of this Act or
section 351 of the Public Health Service Act to use the
patent, trade secret, or any other intellectual
property other than as described in this subsection;
``(B) preventing a sponsor of an application under
section 505 of this Act or section 351 of the Public
Health Service Act from using a different, comparable
aspect of the elements to assure safe use as authorized
under this section;
``(C) in any way negating the applicability of a
risk evaluation and mitigation strategy with elements
to assure safe use, as otherwise required under this
section; or
``(D) limiting the application of any provision of
the antitrust laws (as defined in subsection (a) of the
first section of the Clayton Act (15 U.S.C. 12(a)).''.
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