{"database": "lobbying", "table": "lobbying_activities", "rows": [[590212, "3b17e9e8-061f-4d09-aca8-e1de30ff8d7b", "Q1", "AMERICAN ASSOCIATION FOR JUSTICE", 4733, "AMERICAN ASSOCIATION FOR JUSTICE", 2008, "first_quarter", "HCR", "H.R. 1328/S. 1200 (Indian Health Care Improvement Act; specific interest in authority of the Secretary of HHS under section 213 to promulgate standards for service under the bill.)\n\nMedical Device Safety Act; draft legislation (not introduced as of 03-31-08) to amend the Food Drug and Cosmetic Act to clarify the scope of federal preemption of state law with regard to medical devices.\n\nCongressional lobbying in response to proposed FDA rule regarding supplemental application to update warning labels on prescription drugs, medical devices and biologics.", "Consumer Product Safety Commission (CPSC),HOUSE OF REPRESENTATIVES,SENATE", null, 1130000, 0, 0, "2008-04-15T15:04:45-04:00"]], "columns": ["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"], "primary_keys": ["id"], "primary_key_values": ["590212"], "units": {}, "query_ms": 0.35308103542774916, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}