POLICY DIRECTIONS INC. for BAUSCH & LOMB
What was lobbied
One issue area, each in the filer's own words, with who lobbied on it and where.
Health Issues HCR
510(k) Medical Device Review Process: (No Bills). Issues related to changing the 510(k) structure. FDA regulation of Drugs and/or Medical Devices: HR 759, the FDA Globalization Act. Provisions related to drugs and/or medical devices that affect fees, inspections and import safety. Federal Preemption: S.540/HR1346 - the Medical Device Safety Act of 2009. HR3590, the Patient Protection and Affordable Care Act and HR 3962, Affordable Healthcare for America Act, provisions related to physician reporting requirements, excise tax on medical device companies, and a medical device registry.
| Lobbyist | Covered position, as disclosed |
|---|---|
| NICOLE SUZANNE CHURCHILL | — |
| FRANKIE L TRULL | — |
Shown as published by the Senate Office of Public Records and the House Clerk under the Lobbying Disclosure Act. The official filing is the record; open it for the full form.