{"database": "lobbying", "table": "lobbying_activities", "rows": [[507249, "6669af60-e782-4bd6-bb2b-9c68bf3c2603", "MM", "DENNY MILLER ASSOCIATES", 25328, "CELL THERAPEUTICS", 2007, "mid_year", "MED", "HR 2900, S 1082, FDA Overhaul, all provisions.  HR 1956, Patient Protection and Innovative Biologic Medicines Act of 2007, all provisions.  HR 1038, S 623, Access to Life-Saving Medicine Act, all provisions.  S 1695, Biologics Price Competition and Innovation Act of 2007, all provisions.", "HOUSE OF REPRESENTATIVES,SENATE", 0, 0, "2007-07-30T14:27:42-04:00"]], "columns": ["id", "filing_uuid", "filing_type", "registrant_name", "registrant_id", "client_name", "filing_year", "filing_period", "issue_code", "specific_issues", "government_entities", "is_no_activity", "is_termination", "received_date"], "primary_keys": ["id"], "primary_key_values": ["507249"], "units": {}, "query_ms": 0.366812979336828, "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"}