Lobbying Relationship

Client

Bristol-Myers Squibb

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Lobbying firm

Ogilvy Government Relations

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  • Issues related to the implementation of the Patient Protection and Affordable Care Act, Prescription Drug User Fee Act reauthorization, health care and mental health.
  • Issues related to Medicare and Medicaid.
  • S.3187/H.R.5651, Food and Drug Administration Safety and Innovation Act (Public Law No: 112-144); Medical Device User Fee Act and related issues.

Duration: to

General Issues: Health Issues, Medicare/Medicaid, Medical/Disease Research/Clinical Labs

Spending: about $190,000 (But it's complicated. Here's why.)

Agencies lobbied since 2011: House of Representatives, U.S. Senate

Bills mentioned

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

Sponsor: Tom Harkin (D-Iowa)

H.R.5651: Food and Drug Administration Reform Act of 2012

Sponsor: Fred Upton (R-Mich.)

Show All Mentioned Bills

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 Tilton HCRPolicyCoor/SenPolAdvr:Energy/CommerceComm,Bilirakis
J. Michael Hogan Jr. DepCoS, Ben Nelson; LegDir, Peter Deutsch
John O'Neill PolDir/Coun,SenMinWhip;Couns,SenFinComm
Gordon Taylor COS/LD/Coun,John;Leg Asst/Press Secy,Hayes

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
Q2 Report
Q1 Report
Q4 Report
Q3 Report
Q2 Report
Q1 Report
Registration

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

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