{"database": "openregs", "table": "documents", "rows": [["FDA-2020-D-2307-0052", "FDA", "FDA-2020-D-2307", "Real-World Data: Assessing Electronic Health Records and Medical Claims Data To Support Regulatory Decision-\nMaking for Drug and Biological Products; Draft Guidance for Industry; Reopening of the Comment Period", "Notice", "Notice of Availability", "2021-12-10T05:00:00Z", 2021, 12, "2021-12-10T05:00:00Z", "2022-01-25T04:59:59Z", "2024-07-25T12:53:56Z", "2021-26699", 0, 0, "0900006484eb7ef1"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2020-D-2307-0052"], "units": {}, "query_ms": 41.342971846461296, "source": "Federal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"}