Lobbying Relationship

Client

Amgen USA Inc.

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Lobbying firm

PARRY, ROMANI, DECONCINI & SYMMS

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  • Medicare Part D reimbursement issues dealing with patient payments in the "doughnut hole." No legislation introduced. Monitor PDUFA (Prescription Drug User Fee Act) reauthorization under S. 3187, Food and Drug Administration Safety and Innovation Act.

Duration: to

General Issues: Medicare/Medicaid, Health Issues, Pharmacy

Spending: about $510,000 (But it's complicated. Here's why.)

Agencies lobbied since 2010: U.S. Senate

Bills mentioned

S.3187: Food and Drug Administration Safety and Innovation Act

Sponsor: Tom Harkin (D-Iowa)

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Lobbyists

Lobbyists named here were listed on a filing related to this lobbying engagement. They may not be working on it now. Occasionally, a single lobbyist whose name is spelled two different ways on filings may be represented twice here.

Lobbyist Covered positions?
Steve Symm U.S. Senator: 1981 - 1993
Thaddeus Strom Chief Counsel, Sen. Strom Thurmond: 1987 to 1988 Gen. Coun./Staff Dir., Sen. Cmte. on the Judciary: 1988-1991 Chief Coun/Staff Dir, Sen Cmte on the Judiciary:1991-1993 ChfCoun/StfDir, SenCmteonAntitrust,BusRghts,Etc: 1994-1997
Edward Baxter Chief Counsel and Staff Director, Senate Judiciary Committee's Subcommittee on Patents, Copyrights and Trademarks: 1987 to 1990
James Rock Staff Asst., U.S. House Committee on Budget: 1985 to 2000
Romano Romani n/a
Steve Symms n/a

Disclosures Filed

Once a lobbying engagement begins, the lobbyist or firm is required to file updates four times a year. Those updates sometimes change which lobbyists are involved or add new issues being discussed. When lobbyists stop working for a client, the firm is also supposed to file a report disclosing the end of the relationship.

Termination
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Registration

Source: Clerk of the U.S. House of Representatives and Secretary of the Senate

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