lobbying_activities: 1953530
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1953530 | 734c605d-a7a9-4a99-892e-643ba9086316 | Q1 | APOTEX CORP. | 310973 | APOTEX CORP. | 2017 | first_quarter | PHA | Federal policy relating to the reauthorization of the Generic Drug User Fee Act; Federal policy relating to the cost of prescription pharmaceuticals; Federal policy relating to the provision of brand drug products by brand manufacturers to generic manufacturers for development testing, and for shared Risk Evaluation and Mitigation (REMS) programs for brand and generic pharmaceuticals; HR 749, the Lower Drug Costs Through Competition Act, provisions relating to priority review vouchers for and expedited approval of certain generic drug applications, and Risk Evaluation and Mitigation (REMS) programs; and Draft legislation (no bill number) related to generic drug exclusivity and the review of Abbreviated New Drug Applications (ANDAs). | HOUSE OF REPRESENTATIVES,SENATE | 160000 | 0 | 0 | 2017-04-16T21:04:18.540000-04:00 |