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HOUSE 2891117th CongressOrdered to be Reported in the Nature of a Substitute by the Yeas and Nays: 28 - 13.

Preserve Access to Affordable Generics and Biosimilars Act

Last Action
9/29/2021

Actions

  • 2021-09-29Ordered to be Reported in the Nature of a Substitute by the Yeas and Nays: 28 - 13.
  • 2021-09-29Committee Consideration and Mark-up Session Held.
  • 2021-04-29Referred to the Subcommittee on Health.
  • 2021-04-28Referred to the Committee on the Judiciary, 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.
  • 2021-04-28Referred to the Committee on the Judiciary, 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.
  • 2021-04-28Introduced in House
  • 2021-04-28Introduced in House

CRS Summary

As of 2021-04-28 (00)

Preserve Access to Affordable Generics and Biosimilars Act

This bill authorizes the Federal Trade Commission (FTC) to initiate proceedings against parties to any agreement resolving or settling a patent infringement claim in connection with the sale of a drug or biological product. Such an agreement is presumed to have anticompetitive effects and is a violation of this bill if the filer of the generic drug or biosimilar application receives anything of value and agrees to limit or forego research, development, manufacturing, marketing, or sales of the generic drug or biosimilar.

An agreement is exempted if the only consideration granted to the generic manufacturer is (1) the right to market its product prior to the expiration of any statutory exclusivity, (2) a payment for reasonable litigation expenses, or (3) a covenant not to sue on any claim that the generic drug or biosimilar infringes a patent. An agreement is also exempt if the agreement's pro-competitive benefits outweigh the anticompetitive effects.

When a generic or biosimilar drug manufacturer enters into an agreement with another drug manufacturer related to the manufacturing, marketing, or sale of a drug, the manufacturers must certify that the material they have given the FTC concerning the agreement contains the complete agreement and any agreements related to that main agreement, including descriptions of any oral agreements or representations.

The bill imposes penalties for violations of this bill, including the forfeiture of the 180-day marketing exclusivity period for a generic drug.

Cosponsors (7)

  • David Cicilline (D-RI)
  • Ken Buck (R-CO)
  • CAROLYN MALONEY (D-NY)
  • Burgess Owens (R-UT)
  • ELEANOR NORTON (D-DC)
  • Ted Budd (R-NC)
  • SHEILA JACKSON LEE (D-TX)

Subjects

  • Administrative law and regulatory procedures
  • Civil actions and liability
  • Competition and antitrust
  • Contracts and agency
  • Federal Trade Commission (FTC)
  • Intellectual property
  • Judicial review and appeals
  • Licensing and registrations
  • Manufacturing
  • Marketing and advertising
  • Prescription drugs
Read on Congress.gov

Sourced from Congress.gov (public domain).

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.