{"database": "lobbying", "table": "lobbying_activities", "rows": [[2152005, "6ab9d39a-e1e2-460f-9ccc-8161afac0705", "Q2", "HOOPER, LUNDY & BOOKMAN, P.C.", 401020884, "ROCHE DIAGNOSTICS CORPORATION", 2018, "second_quarter", "MED", "Diagnostic Accuracy & Innovation Act (DAIA) Duiscussion Draft.", "HOUSE OF REPRESENTATIVES,SENATE", 50000, null, 0, 0, "2018-07-18T17:55:01.807000-04:00"]], "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": ["2152005"], "units": {}, "query_ms": 112.12504282593727, "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"}