documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
15 rows where docket_id = "FDA-2008-D-0610" sorted by posted_date descending
This data as json, CSV (advanced)
Suggested facets: subtype, posted_date, posted_month, comment_start_date, comment_end_date, open_for_comment, withdrawn, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)
document_type 3
agency_id 1
- FDA 15
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2008-D-0610-0021 | FDA | None FDA-2008-D-0610 | Guidance Documents Related to Coronavirus Disease 2019 (COVID–19) | Notice | General Notice | 2023-03-13T04:00:00Z | 2023 | 3 | 2023-03-13T04:00:00Z | 2023-03-13T14:07:53Z | 2023-05094 | 0 | 0 | 090000648579b2d6 | |
| FDA-2008-D-0610-0020 | FDA | None FDA-2008-D-0610 | Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During a Pandemic - Guidance for Industry | Other | Guidance | 2020-05-08T04:00:00Z | 2020 | 5 | 2020-05-08T04:00:00Z | 2024-12-18T13:51:32Z | 1 | 0 | 0900006484591e76 | ||
| FDA-2008-D-0610-0018 | FDA | None FDA-2008-D-0610 | Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During a Pandemic; Guidance for Industry | Other | Guidance | 2020-03-19T04:00:00Z | 2020 | 3 | 2020-03-19T04:00:00Z | 2024-11-12T23:18:22Z | 1 | 0 | 0900006484465441 | ||
| FDA-2008-D-0610-0017 | FDA | None FDA-2008-D-0610 | Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During a Pandemic; Guidance for Industry | Other | 2020-03-19T00:00:00Z | 2020 | 3 | 2020-04-21T06:12:28Z | 0 | 1 | 090000648445772a | ||||
| FDA-2008-D-0610-0016 | FDA | None FDA-2008-D-0610 | Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals | Notice | Notice of Approval | 2018-06-19T04:00:00Z | 2018 | 6 | 2018-06-19T04:00:00Z | 2018-06-19T18:46:08Z | 2018-13098 | 0 | 0 | 090000648342f63c | |
| FDA-2008-D-0610-0015 | FDA | None FDA-2008-D-0610 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic | Notice | 30 Day Proposed Information Collection | 2018-04-09T04:00:00Z | 2018 | 4 | 2018-04-09T04:00:00Z | 2018-05-10T03:59:59Z | 2018-04-09T15:36:56Z | 2018-07154 | 0 | 0 | 09000064830dd395 |
| FDA-2008-D-0610-0013 | FDA | None FDA-2008-D-0610 | Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic | Notice | 60 Day Proposed Information Collection | 2017-10-31T04:00:00Z | 2017 | 10 | 2017-10-31T04:00:00Z | 2018-01-03T04:59:59Z | 2017-11-01T01:03:17Z | 2017-23659 | 0 | 0 | 0900006482c28640 |
| FDA-2008-D-0610-0012 | FDA | None FDA-2008-D-0610 | Guidance For Industry on Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic | Other | Guidance | 2012-02-24T05:00:00Z | 2012 | 2 | 2012-02-24T05:00:00Z | 2012-02-24T15:11:42Z | 0 | 0 | 0900006480fc051a | ||
| FDA-2008-D-0610-0011 | FDA | None FDA-2008-D-0610 | Guidance For Industry on Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic; Availability | Notice | Notice of Availability | 2012-02-24T05:00:00Z | 2012 | 2 | 2012-02-24T05:00:00Z | 2012-02-24T14:57:14Z | 2012-04288 | 0 | 0 | 0900006480fc01ae | |
| FDA-2008-D-0610-0010 | FDA | None FDA-2008-D-0610 | Agency Information Collection Activities; Proposals, Submissions, and Approvals: Draft Guidance for Industry on Postmarketing Adverse Event Reporting for Medical Products, etc. | Notice | General Notice | 2011-06-24T04:00:00Z | 2011 | 6 | 2011-06-24T04:00:00Z | 2011-07-26T03:59:59Z | 2011-06-24T18:53:04Z | 2011-15799 | 0 | 0 | 0900006480eb3446 |
| FDA-2008-D-0610-0009 | FDA | None FDA-2008-D-0610 | Guidance for Industry Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic | Other | GDL-Guidance (Supporting and Related Materials) | 2011-01-10T05:00:00Z | 2011 | 1 | 2011-01-10T05:00:00Z | 2011-03-09T04:59:59Z | 2020-03-19T19:31:38Z | 0 | 0 | 0900006480bc6e66 | |
| FDA-2008-D-0610-0008 | FDA | None FDA-2008-D-0610 | Draft Guidance for Industry; Availability Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic | Notice | NAD-Notice of Availability of Data | 2011-01-07T05:00:00Z | 2011 | 1 | 2011-01-07T05:00:00Z | 2011-03-09T04:59:59Z | 2011-03-03T20:47:47Z | 2011-00094 | 0 | 0 | 0900006480bc6d37 |
| FDA-2008-D-0610-0006 | FDA | None FDA-2008-D-0610 | See FDA-2008-D-0610-0004 | Supporting & Related Material | C-Comment (Supporting and Related Material) | 2009-02-20T05:00:00Z | 2009 | 2 | 2009-02-20T16:38:45Z | 0 | 0 | 090000648085cb0a | |||
| FDA-2008-D-0610-0002 | FDA | None FDA-2008-D-0610 | Guidance for Industry - Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic - Draft Guidance | Other | GDL-Guidance (Supporting and Related Materials) | 2008-12-16T05:00:00Z | 2008 | 12 | 2009-02-19T17:57:41Z | 0 | 0 | 09000064807ddc44 | |||
| FDA-2008-D-0610-0001 | FDA | None FDA-2008-D-0610 | Draft Guidance for Industry on Postmarketing Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic; Availability | Notice | NAD-Notice of Availability of Data | 2008-12-16T05:00:00Z | 2008 | 12 | 2008-12-16T05:00:00Z | 2009-02-18T04:59:59Z | 2009-02-19T17:59:49Z | 0 | 0 | 09000064807ddbf2 |
Advanced export
JSON shape: default, array, newline-delimited, object
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;