documents
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)
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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;