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Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

11 rows where docket_id = "FDA-2011-N-0231" sorted by posted_date descending

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Suggested facets: subtype, posted_month, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)

posted_year 6

  • 2011 3
  • 2014 2
  • 2018 2
  • 2021 2
  • 2017 1
  • 2020 1

document_type 1

  • Notice 11

agency_id 1

  • FDA 11
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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2011-N-0231-0015 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals Notice Notice of Approval 2021-05-19T04:00:00Z 2021 5 2021-05-19T04:00:00Z   2023-09-07T21:10:22Z 2021-10535 0 0 0900006484b1b36a
FDA-2011-N-0231-0013 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 30 Day Proposed Information Collection 2021-02-23T05:00:00Z 2021 2 2021-02-23T05:00:00Z 2021-03-26T03:59:59Z 2023-09-07T21:09:23Z 2021-03541 0 0 0900006484a47c79
FDA-2011-N-0231-0011 FDA None FDA-2011-N-0231 Agency Information Collection Activities: Proposed Collection; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 60 Day Proposed Information Collection 2020-09-01T04:00:00Z 2020 9 2020-09-01T04:00:00Z 2020-11-03T04:59:59Z 2023-09-07T21:08:45Z 2020-19239 0 0 090000648482d8bb
FDA-2011-N-0231-0010 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals Notice Notice of Approval 2018-06-08T04:00:00Z 2018 6 2018-06-08T04:00:00Z   2023-09-07T21:07:07Z 2018-12338 0 0 090000648337b830
FDA-2011-N-0231-0009 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 30 Day Proposed Information Collection 2018-01-08T05:00:00Z 2018 1 2018-01-08T05:00:00Z 2018-02-08T04:59:59Z 2023-09-07T21:06:53Z 2018-00095 0 0 0900006482db13e0
FDA-2011-N-0231-0008 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 60 Day Proposed Information Collection 2017-07-18T04:00:00Z 2017 7 2017-07-18T04:00:00Z 2017-09-19T03:59:59Z 2023-09-07T21:06:37Z 2017-15004 0 0 090000648293b6b2
FDA-2011-N-0231-0007 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 30 Day Proposed Information Collection 2014-10-29T04:00:00Z 2014 10 2014-10-29T04:00:00Z 2014-11-29T04:59:59Z 2014-11-28T03:00:48Z 2014-25637 0 0 0900006481905358
FDA-2011-N-0231-0005 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Experience Reporting for Licensed Biological Products; and General Records Notice 60 Day Proposed Information Collection 2014-04-07T04:00:00Z 2014 4 2014-04-07T04:00:00Z 2014-06-07T03:59:59Z 2014-10-16T21:34:25Z 2014-07711 0 0 09000064816a301b
FDA-2011-N-0231-0004 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice Notice of Approval 2011-11-25T05:00:00Z 2011 11 2011-11-25T05:00:00Z   2011-11-25T14:16:51Z 2011-30326 0 0 0900006480f73634
FDA-2011-N-0231-0003 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Adverse Experience Reporting for Licensed Biological Products; and General Records Notice General Notice 2011-07-14T04:00:00Z 2011 7 2011-07-14T04:00:00Z 2011-08-16T03:59:59Z 2011-07-14T13:39:05Z 2011-17675 0 0 0900006480ec1c64
FDA-2011-N-0231-0001 FDA None FDA-2011-N-0231 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Adverse Experience Reporting for Licensed Biological Products and General Records Notice N-Notice 2011-04-21T04:00:00Z 2011 4 2011-04-21T04:00:00Z 2011-06-21T03:59:59Z 2011-04-21T13:59:28Z 2011-09651 0 0 0900006480c34c8b

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CREATE TABLE documents (
    id TEXT PRIMARY KEY,
    agency_id TEXT,
    docket_id TEXT REFERENCES dockets(id),
    title TEXT,
    document_type TEXT,
    subtype TEXT,
    posted_date TEXT,
    posted_year INTEGER,
    posted_month INTEGER,
    comment_start_date TEXT,
    comment_end_date TEXT,
    last_modified TEXT,
    fr_doc_num TEXT,
    open_for_comment INTEGER,
    withdrawn INTEGER,
    object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;
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