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All lobbying filings

COVINGTON & BURLING LLP

Lobbying for PHARMACEUTICAL RESEARCH & MANUFACTURERS OF AMERICA INC

 Filing 3rd Quarter - Report
3rd Quarter (July 1 - Sep 30) 2025 · District of Columbia · Senate · $130,000.00 income · posted Oct 20, 2025

Official filing document

 Bills named in this filing 11
  • S 863
    Genomic Data Protection Act
  • S 2620
    REMEDY Act
  • S 355
    FDA Modernization Act 3.0
  • HR 2821
    FDA Modernization Act 3.0
  • S 2296
    National Defense Authorization Act for Fiscal Year 2026
  • S 1097
    Interagency Patent Coordination and Improvement Act of 2025
  • S 2658
    Medication Affordability and Patent Integrity Act
  • S 1414
    Expedited Access to Biosimilars Act
  • S 1954
    Biosimilar Red Tape Elimination Act
  • HR 5526
    Biosimilar Red Tape Elimination Act
  • S 2256
    Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations Act, 2026
 Lobbying activity 2
Copyright/Patent/Trademark

Issues related to biopharmaceutical innovation and intellectual property (no bill); issues related to intellectual property and Bayh-Dole in the Genomic Data Protection Act (S. 863 / no House bill); induced infringement.

Health Issues

Proposed amendments to the Inflation Reduction Act (P.L. 117-169); Biosimilars Access and Affordability Act (no bill number); REMEDY Act (S. 2620); FDA Modernization Act 3.0 (S. 355 / H.R. 2821); issues related to reauthorization of the Prescription Drug User Fee Act (no bill); proposed amendment to the National Defense Authorization Act for Fiscal Year 2026 (S.Amdt.3236 to S.2296); issues related to vaccine access (no bill); Interagency Patent Coordination and Improvement Act of 2025 (S. 1097); Medication Affordability and Patent Integrity Act (S. 2658 / no House bill); Expedited Access to Biosimilars Act (S. 1414); Biosimilar Red Tape Elimination Act (S. 1954, HR 5526); Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations Act, 2026 (S.2256); conditional approval; orphan-drug exclusivity; FDA reform.

Source: federal Lobbying Disclosure Act filing. Bills are parsed from the activity descriptions.

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