documents

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

5 rows where docket_id = "FDA-2012-N-0921" sorted by posted_date descending

✎ View and edit SQL

This data as json, CSV (advanced)

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

posted_year 4

document_type 1

agency_id 1

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posted_date ▲ posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2012-N-0921-0005 FDA None FDA-2012-N-0921 Agency Information Collection Activities; Proposals, Submissions, and Approvals Notice Notice of Approval 2016-08-10T04:00:00Z 2016 8 2016-08-10T04:00:00Z   2016-08-10T14:27:04Z 2016-19021 0 0 0900006482165241
FDA-2012-N-0921-0004 FDA None FDA-2012-N-0921 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Event Reporting; Electronic Submissions Notice 30 Day Proposed Information Collection 2016-02-29T05:00:00Z 2016 2 2016-02-29T05:00:00Z 2016-03-31T03:59:59Z 2016-03-02T19:19:29Z 2016-04223 0 0 0900006481e8f9af
FDA-2012-N-0921-0003 FDA None FDA-2012-N-0921 Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Event Reporting; Electronic Submissions Notice 60 Day Proposed Information Collection 2015-11-18T05:00:00Z 2015 11 2015-11-18T05:00:00Z 2016-01-20T04:59:59Z 2015-11-18T16:39:20Z 2015-29407 0 0 0900006481d54910
FDA-2012-N-0921-0002 FDA None FDA-2012-N-0921 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Electronic Submission of Food and Drug Administration Adverse Event Reports and Other Safety Information Using the Electronic Submission Gateway and the Safety Reporting Portal Notice 30 Day Proposed Information Collection 2013-01-16T05:00:00Z 2013 1 2013-01-16T05:00:00Z 2013-02-16T04:59:59Z 2015-11-10T18:54:10Z 2013-00761 0 0 09000064811c05ba
FDA-2012-N-0921-0001 FDA None FDA-2012-N-0921 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Electronic Submission of Food and Drug Administration Adverse Event Reports and Other Safety Information Using the Electronic Submission Gateway and the Safety Reporting Portal Notice 60 Day Proposed Information Collection 2012-09-14T04:00:00Z 2012 9 2012-09-14T04:00:00Z 2012-11-14T04:59:59Z 2015-11-10T18:53:41Z 2012-22659 0 0 0900006481117417

Advanced export

JSON shape: default, array, newline-delimited, object

CSV options: 

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;