lobbying_activities: 583856
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | filing_uuid | filing_type | registrant_name | registrant_id | client_name | filing_year | filing_period | issue_code | specific_issues | government_entities | income_amount | expense_amount | is_no_activity | is_termination | received_date |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 583856 | c8c02fc9-9a2c-43df-a103-e4ba07510513 | MA | EASTMAN KODAK COMPANY | 13016 | EASTMAN KODAK COMPANY | 2007 | mid_year | HCR | S. 1082 Prescription Drug User Fee Amendments of 2007. Advocating for reforms to the Third Party Inspection program to allow flexibility among certified organizations and reforms to the formulas used to calculate user fees paid to FDA for medical device reviews to cap the annual increases in the fees and after more predictability in the rate of increase yearly. Generic Biologics - H.R. 1038, H.R. 1432, S. 623, Retiree Health Care (no legislation as of yet), Healthy Workforce Act S. 1342 | 300000 | 0 | 0 | 2012-05-03T13:17:05.657000-04:00 |