{"database": "lobbying", "table": "lobbying_activities", "rows": [[1264069, "a40be5bb-9281-4015-b028-b45344fa5a88", "Q2", "MEHLMAN CONSULTING, INC.", 284950, "AMERICAN CLINICAL LABORATORY ASSOCIATION", 2012, "second_quarter", "MED", "Health reform law implementation issues including application of medical device tax to clinical laboratory tests and laboratory fee schedule.      In-office ancillary services exception to Stark Law.    \nH.R. 3207, The Modernizing Laboratory Test Standards for Patients Act.                 \nH.R. 5651, Food and Drug Administration Reform Act      S. 3187, Food and Drug Administration Safety and Innovation Act.", "Health & Human Services, Dept of (HHS),HOUSE OF REPRESENTATIVES,Office of Management & Budget (OMB),SENATE", 60000, null, 0, 0, "2012-07-16T13:15:06.857000-04:00"]], "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": ["1264069"], "units": {}, "query_ms": 0.32774399733170867, "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"}