{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\" and docket_id = \"FDA-1997-N-0103\" sorted by posted_date descending", "rows": [["FDA-1997-N-0103-0107", "FDA", "FDA-1997-N-0103", "Reference 3 Biological Product Deviation Report Form (Form FDA-3486) and Instructions re: Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:24:02Z", null, 0, 0, "0900006481e36f00"], ["FDA-1997-N-0103-0106", "FDA", "FDA-1997-N-0103", "Reference 2: Presidential Memorandum on Plain Language, June 1, 1998 re: Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:19:13Z", null, 0, 0, "0900006481e36eff"], ["FDA-1997-N-0103-0108", "FDA", "FDA-1997-N-0103", "Reference 4: Internet Biological Product Deviation Report Instructions and Screen Examples re: Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:28:17Z", null, 0, 0, "0900006481e36f01"], ["FDA-1997-N-0103-0110", "FDA", "FDA-1997-N-0103", "Supporting Statement: Biological Products: Reporting of Biological Product Deviations in Manufacturing OMB No. 0910-0458", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:36:48Z", null, 0, 0, "0900006481e3747d"], ["FDA-1997-N-0103-0103", "FDA", "FDA-1997-N-0103", "Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Notice", "Notice of Final Rule", "2016-01-28T05:00:00Z", 2016, 1, "2016-01-28T05:00:00Z", "2001-05-05T03:59:59Z", "2016-01-28T17:06:52Z", null, 0, 0, "09000064805d070a"], ["FDA-1997-N-0103-0109", "FDA", "FDA-1997-N-0103", "Agency Information Collection Activities; Announcement of OMB Approval; Biological Products: Reporting of Biological Product Deviations in Manufacturing; Notice", "Notice", "Notice of Approval", "2016-01-28T05:00:00Z", 2016, 1, "2016-01-28T05:00:00Z", null, "2016-01-28T17:32:36Z", null, 0, 0, "09000064805d070c"], ["FDA-1997-N-0103-0104", "FDA", "FDA-1997-N-0103", "List of References re: Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:11:58Z", null, 0, 0, "0900006481e36f02"], ["FDA-1997-N-0103-0105", "FDA", "FDA-1997-N-0103", "Reference 1: Memorandum from Inspector General to DHHS, May 31, 1995 re: Biological Products: Reporting of Biological Product Deviations in Manufacturing; Final Rule", "Supporting & Related Material", "Background Material", "2016-01-28T05:00:00Z", 2016, 1, null, null, "2016-01-28T17:15:49Z", null, 0, 0, "0900006481e36efe"], ["FDA-1997-N-0103-0065", "FDA", "FDA-1997-N-0103", "Appendix A American Red Cross Blood Services Error and Accident Report re: Comment from American Red Cross", "Supporting & Related Material", "Background Material", "2016-01-20T05:00:00Z", 2016, 1, null, null, "2016-01-20T15:25:49Z", null, 0, 0, "0900006481e21228"], ["FDA-1997-N-0103-0051", "FDA", "FDA-1997-N-0103", "Attachment 1 Sample of Administrative Procedure re: Comment from University of California, Davis", "Supporting & Related Material", "Background Material", "2016-01-20T05:00:00Z", 2016, 1, null, null, "2016-01-20T14:21:28Z", null, 0, 0, "0900006481e20afd"], ["FDA-1997-N-0103-0066", "FDA", "FDA-1997-N-0103", "Appendix B Instructions for Completing the American Red Cross re: Appendix A American Red Cross Blood Services Error and Accident Report re: Comment from American Red Cross", "Supporting & Related Material", "Background Material", "2016-01-20T05:00:00Z", 2016, 1, null, null, "2016-01-20T15:31:05Z", null, 0, 0, "0900006481e21227"], ["FDA-1997-N-0103-0062", "FDA", "FDA-1997-N-0103", "Attachment 1 AABB Written Comments on the Information Collection Provisions re: Comment from William Beaumont Hospital", "Supporting & Related Material", "Background Material", "2016-01-20T05:00:00Z", 2016, 1, null, null, "2016-01-20T15:05:33Z", null, 0, 0, "0900006481e20eff"], ["FDA-1997-N-0103-0047", "FDA", "FDA-1997-N-0103", "Attachment 1 Comment from AABB Dated October 22, 1997 re: Comment from American Association of Blood Banks", "Supporting & Related Material", "Background Material", "2016-01-19T05:00:00Z", 2016, 1, null, null, "2016-01-19T19:47:04Z", null, 0, 0, "0900006481e1b614"], ["FDA-1997-N-0103-0001", "FDA", "FDA-1997-N-0103", "Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Proposed Rule", "Notice of Proposed Rulemaking (NPRM)", "2016-01-13T05:00:00Z", 2016, 1, "1997-09-23T04:00:00Z", "1997-12-23T04:59:59Z", "2016-01-13T16:47:30Z", null, 0, 0, "09000064805d06a5"], ["FDA-1997-N-0103-0006", "FDA", "FDA-1997-N-0103", "Tab D Error and Accident Report - Annual Summary for FY 96 re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T17:08:48Z", null, 0, 0, "0900006481e07e23"], ["FDA-1997-N-0103-0007", "FDA", "FDA-1997-N-0103", "Tab E GAO Blood Supply FDA Oversight and Remaining Issues of Safety February 1997 re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T17:12:21Z", null, 0, 0, "0900006481e07e24"], ["FDA-1997-N-0103-0002", "FDA", "FDA-1997-N-0103", "List of References re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T16:51:43Z", null, 0, 0, "09000064805d0709"], ["FDA-1997-N-0103-0003", "FDA", "FDA-1997-N-0103", "Tab A Memorandum from FDA CBER to All Registered Blood Establishments List of References re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T16:56:17Z", null, 0, 0, "09000064805d070b"], ["FDA-1997-N-0103-0004", "FDA", "FDA-1997-N-0103", "Tab B Report from DHHS OIG \"Reporting Process for Blood Establishments to Notify the Food and Drug Administration of Errors an Accidents Affecting Blood\" re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T17:00:09Z", null, 0, 0, "0900006481e07d7a"], ["FDA-1997-N-0103-0005", "FDA", "FDA-1997-N-0103", "Tab C Federal Register Notice Guideline for Quality Assurance in Blood (60FR36290) July 11, 1995 re: Biological Products; Reporting of Errors and Accidents in Manufacturing; Proposed Rule", "Supporting & Related Material", "Background Material", "2016-01-13T05:00:00Z", 2016, 1, null, null, "2016-01-13T17:05:03Z", null, 0, 0, "0900006481e07d7b"]], "truncated": false, "filtered_table_rows_count": 20, "expanded_columns": [], "expandable_columns": [[{"column": "docket_id", "other_table": "dockets", "other_column": "id"}, "title"]], "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"], "units": {}, "query": {"sql": "select 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 from documents where \"agency_id\" = :p0 and \"docket_id\" = :p1 order by posted_date desc limit 101", "params": {"p0": "FDA", "p1": "FDA-1997-N-0103"}}, "facet_results": {"agency_id": {"name": "agency_id", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103", "results": [{"value": "FDA", "label": "FDA", "count": 20, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-1997-N-0103", "selected": true}], "truncated": false}, "document_type": {"name": "document_type", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103", "results": [{"value": "Supporting & Related Material", "label": "Supporting & Related Material", "count": 17, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&document_type=Supporting+%26+Related+Material", "selected": false}, {"value": "Notice", "label": "Notice", "count": 2, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&document_type=Notice", "selected": false}, {"value": "Proposed Rule", "label": "Proposed Rule", "count": 1, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&document_type=Proposed+Rule", "selected": false}], "truncated": false}, "posted_year": {"name": "posted_year", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103", "results": [{"value": 2016, "label": 2016, "count": 20, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&posted_year=2016", "selected": false}], "truncated": false}}, "suggested_facets": [{"name": "subtype", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet=subtype"}, {"name": "posted_date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet=posted_date"}, {"name": "comment_start_date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet=comment_start_date"}, {"name": "posted_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet_date=posted_date"}, {"name": "comment_start_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet_date=comment_start_date"}, {"name": "comment_end_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet_date=comment_end_date"}, {"name": "last_modified", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?agency_id=FDA&docket_id=FDA-1997-N-0103&_facet_date=last_modified"}], "next": null, "next_url": null, "private": false, "allow_execute_sql": true, "query_ms": 785.8472259249538, "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"}