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1st Quarter - Report · 2026

Filing UUID
de6ea471-2bb4-44d0-a42c-d12b00f99a28
Type
Q1 — 1st Quarter - Report
Period
first_quarter
Year
2026
Posted
2026-04-20 17:30:23
Income (reported)
Expenses (reported)
$1,070,000
Expenses method
A
Filing document
Open on lda.senate.gov
Registrant (lobbying firm)

FRESENIUS KABI USA LLC

Generic and Biosimilar pharmaceutical manufacturer

Contact
SARAH D'ORSIE
Phone
+1 717-487-6362
Address
zip:60047, city:Lake Zurich, state:IL, street:Three Corporate Drive
Client

FRESENIUS KABI USA LLC

State
IL
Country
US
Government-entity client
false
Effective date
2020-08-12
Issues lobbied + lobbyists (6)

TRD — Trade (domestic/foreign)

Medical Device Safety Biosimilar Tariffs and USPTO Proposed Rule PTAB Proposed Rule - Restrict Use of IPR FY27 Appropriations: Domestic Production of Essential Medicines; Chemical-free Medical Devices Federal Procurement Preferences for Domestic Medicines Clinical Trials for Biosimilars; Interchangeability Biosimilar Market Entry through Regulatory Streamlining Biopharmaceutical Manufacturing Preparedness Consortium (BioMaP) Industrial Base Management and Supply Chain (IBMSC)

Lobbyists:

Government entities lobbied: Commerce, Dept of (DOC); Food & Drug Administration (FDA); Health & Human Services, Dept of (HHS); HOUSE OF REPRESENTATIVES; SENATE; U.S. Trade Representative (USTR); White House Office

MMM — Medicare/Medicaid

CMS Preference for Domestic Essential Medicines Net Elective Cost Policy: PBM Reform Through Bid Transparency

Lobbyists:

Government entities lobbied: Centers For Medicare and Medicaid Services (CMS); HOUSE OF REPRESENTATIVES; Labor, Dept of (DOL); SENATE; White House Office

HCR — Health Issues

S. 2276/H.R. 3269: Eliminating Thickets to Increase Competition (ETHIC) Act S. 2296: National Defense Authorization Act (NDAA) for Fiscal Year 2026 Biosimilar Tariffs and USPTO Proposed Rule PTAB Proposed Rule - Restrict Use of IPR Medical Device Safety FDA Streamlining FY27 Appropriations: Domestic Production of Essential Medicines; Chemical-free Medical Devices Clinical Trials for Biosimilars; Interchangeability Biosimilar Market Entry through Regulatory Streamlining FY27 National Defense Authorization Act - Domestic Production of Essential Medicines CMS Preference for Domestic Essential Medicines Federal Procurement Preferences for Domestic Medicines Ancillary Product Patent Reform Net Elective Cost Policy: PBM Reform Through Bid Transparency Biopharmaceutical Manufacturing Preparedness Consortium (BioMaP) Industrial Base Management and Supply Chain (IBMSC) Procurement

Lobbyists:

Government entities lobbied: Centers For Medicare and Medicaid Services (CMS); Commerce, Dept of (DOC); Food & Drug Administration (FDA); HOUSE OF REPRESENTATIVES; Labor, Dept of (DOL); Natl Economic Council (NEC); Patent & Trademark Office (PTO); SENATE; U.S. Trade Representative (USTR); Veterans Affairs, Dept of (VA); White House Office

MAN — Manufacturing

Domestic Manufacturing CMS Preference for Domestic Essential Medicines Biopharmaceutical Manufacturing Preparedness Consortium (BioMaP) Industrial Base Management and Supply Chain (IBMSC)

Lobbyists:

Government entities lobbied: Commerce, Dept of (DOC); Defense, Dept of (DOD); Health & Human Services, Dept of (HHS); HOUSE OF REPRESENTATIVES; Natl Economic Council (NEC); SENATE; White House Office

CPT — Copyright/Patent/Trademark

PTAB Proposed Rule - Restrict Use of IPR Patent Legislation Ancillary Product Patent Reform Clinical Trials for Biosimilars; Interchangeability Biosimilar Market Entry through Regulatory Streamlining

Lobbyists:

Government entities lobbied: Commerce, Dept of (DOC); Food & Drug Administration (FDA); HOUSE OF REPRESENTATIVES; Patent & Trademark Office (PTO); SENATE; U.S. Trade Representative (USTR)

TAX — Taxation/Internal Revenue Code

Tax Incentives for Domestic Manufacturing Tax Credits for Domestic Manufacturing of Essential Medicines

Lobbyists:

Government entities lobbied: HOUSE OF REPRESENTATIVES; SENATE

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