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HR 890 · in committee · significant

Stopping Pharma’s Ripoffs and Drug Savings For All Act

What this bill does

  • The bill requires drug patent owners to prove each patent covers a distinct invention or lose all patents when the first one expires.
  • Pharmaceutical companies and generic drug manufacturers are affected by new patent validity standards.
  • The USPTO must review and reform its drug patent examination procedures to prevent duplicate patents.

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Community Threads

Started by Cosponsor

  1. 01

    How would requiring pharmaceutical companies to prove each patent covers a distinct invention affect the timeline and cost of bringing new drugs to market?

  2. 02

    What evidence exists that duplicate drug patents currently delay generic drug entry and raise medication costs for consumers?

  3. 03

    Which stakeholders—patients, generic manufacturers, or brand-name companies—would face the greatest burden under the USPTO's new patent examination standards?

Cosponsor writes these to seed civic discussion — they aren't user posts. Sign in to reply.

Sponsor · D-NY-18

Patrick Ryan

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Introduced 2025-01-31

Legislative timeline

  1. 2025-01-31 · house · IntroReferral

    Referred to the House Committee on the Judiciary.

  2. 2025-01-31 · IntroReferral

    Introduced in House

  3. 2025-01-31 · IntroReferral

    Introduced in House

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