{"database": "openregs", "table": "dockets", "rows": [["FDA-2020-D-2307", "FDA", "Real-World Data: Assessing Electronic Health Records and Medical Claims Data to Support Regulatory Decision-Making for Drug and Biological Products; Draft Guidance for Industry; Availability", "Nonrulemaking", "2026-06-11T16:25:00Z", "0b000064849a59b3"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2020-D-2307"], "units": {}, "query_ms": 0.25627302238717675, "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"}