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All lobbying filings

COVINGTON & BURLING LLP

Lobbying for PHARMACEUTICAL RESEARCH & MANUFACTURERS OF AMERICA INC

 Filing 2nd Quarter - Report
2nd Quarter (Apr 1 - June 30) 2026 · District of Columbia · $220,000.00 income · posted Jul 20, 2026

Official filing document

 Bills named in this filing 10
  • S 1097
    Interagency Patent Coordination and Improvement Act of 2025
  • S 2658
    Medication Affordability and Patent Integrity Act
  • HR 7953
    FAIR ACT
  • S 3014
    Ensuring Timely Access to Generics Act of 2025
  • S 1095
    Stop STALLING Act
  • HR 8646
    Agriculture, Rural Development, Food and Drug Administration, and Related Agency Appropriations Act, 2027
  • S 1954
    Biosimilar Red Tape Elimination Act
  • HR 5526
    Biosimilar Red Tape Elimination Act
  • S 1414
    Expedited Access to Biosimilars Act
  • HR 2715
    Destruction of Hazardous Imports Act
 Lobbying activity 2
Copyright/Patent/Trademark

Interagency Patent Coordination and Improvement Act of 2025 (S. 1097); Medication Affordability and Patent Integrity Act (S. 2658); Biopharmaceutical policy issues.

Health Issues

Proposed amendments to the Inflation Reduction Act (P.L. 117-169); Fast-tracking Approval for Innovative Rare disease therapies (FAIR) Act (H.R. 7953); Ensuring Timely Access to Generics Act of 2025 (S. 3014); Stop STALLING Act (S. 1095); Food & Drug Administration Fiscal Year 2027 Legislative Proposals; Agriculture, Rural Development, Food and Drug Administration, and Related Agency Appropriations Act, 2027 (H.R. 8646); Medication Affordability and Patent Integrity Act (S. 2658); Biosimilar Red Tape Elimination Act (S. 1954/H.R. 5526); Expedited Access to Biosimilars Act (S. 1414); Clinical trial regulation; Securing Essential Components for U.S. Readiness in Essential Pharmaceuticals (SECURE Rx) Act of 2026 (discussion draft); Securing Innovation and Research from Adversaries (discussion draft); amendments to the National Childhood Vaccine Injury Act of 1986 and the Vaccine Injury Compensation Program; Destruction of Hazardous Imports Act (H.R. 2715); potential amendments to drug country of origin labeling requirements (discussion draft).

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

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