{"database": "openregs", "table": "documents", "rows": [["FDA-2015-D-0390-0025", "FDA", "FDA-2015-D-0390", "Use of Electronic Informed Consent\u2014Questions and Answers; Guidance for Institutional Review Boards, Investigators, and Sponsors; Availability", "Notice", "Notice of Availability", "2016-12-15T05:00:00Z", 2016, 12, "2016-12-15T05:00:00Z", null, "2016-12-15T15:09:26Z", "2016-30146", 0, 0, "090000648240b6b5"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2015-D-0390-0025"], "units": {}, "query_ms": 11.99036801699549, "source": "Federal Register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"}