documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
7 rows where docket_id = "FDA-2017-D-6784" sorted by posted_date descending
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Suggested facets: subtype, posted_date, posted_month, comment_start_date, open_for_comment, posted_date (date), comment_start_date (date), comment_end_date (date), last_modified (date)
document_type 3
agency_id 1
- FDA 7
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2017-D-6784-0014 | FDA | None FDA-2017-D-6784 | Manufacture of Blood Components Using a Pathogen Reduction Device in Blood Establishments: Questions and Answers | Other | Guidance | 2021-11-04T04:00:00Z | 2021 | 11 | 2021-11-04T04:00:00Z | 2024-11-07T00:34:15Z | 1 | 0 | 0900006484e1b788 | ||
| FDA-2017-D-6784-0013 | FDA | None FDA-2017-D-6784 | Manufacture of Blood Components Using a Pathogen Reduction Device in Blood Establishments: Questions and Answers; Guidance for Industry; Availability | Notice | Notice of Availability | 2021-11-04T04:00:00Z | 2021 | 11 | 2021-11-04T04:00:00Z | 2021-11-09T17:41:05Z | 2021-24073 | 0 | 0 | 0900006484e17ebf | |
| FDA-2017-D-6784-0002 | FDA | None FDA-2017-D-6784 | Implementation of Pathogen Reduction Technology in the Manufacture of Blood Components in Blood Establishments: Questions and Answers Draft Guidance for Industry | Other | Guidance | 2017-12-27T05:00:00Z | 2017 | 12 | 2017-12-27T05:00:00Z | 2018-03-28T03:59:59Z | 2024-11-07T01:15:33Z | 1 | 0 | 0900006482d77d2d | |
| FDA-2017-D-6784-0001 | FDA | None FDA-2017-D-6784 | Implementation of Pathogen Reduction Technology in the Manufacture of Blood Components in Blood Establishments: Questions and Answers; Draft Guidance for Industry; Availability | Notice | Notice of Availability | 2017-12-27T05:00:00Z | 2017 | 12 | 2017-12-27T05:00:00Z | 2018-03-28T03:59:59Z | 2018-03-29T01:05:21Z | 2017-28043 | 0 | 0 | 0900006482d76311 |
| FDA-2017-D-6784-0003 | FDA | None FDA-2017-D-6784 | 01 Reference 1 Revised Recommendations for Reducing the Risk of Zika Virus Transmission by Blood and Blood Components; Guidance for Industry | Supporting & Related Material | Background Material | 2017-12-27T05:00:00Z | 2017 | 12 | 2017-12-27T18:06:42Z | 0 | 0 | 0900006482d77d2f | |||
| FDA-2017-D-6784-0005 | FDA | None FDA-2017-D-6784 | 03 Reference 3 Guidance for Industry Pre-Storage Leukocyte Reduction of Whole Blood and Blood Components Intended for Transfusion | Supporting & Related Material | Background Material | 2017-12-27T05:00:00Z | 2017 | 12 | 2017-12-27T18:07:24Z | 0 | 0 | 0900006482d77d31 | |||
| FDA-2017-D-6784-0004 | FDA | None FDA-2017-D-6784 | 02 Reference 2 Guidance for Industry and FDA Review Staff Collection of Platelets by Automated Methods | Supporting & Related Material | Background Material | 2017-12-27T05:00:00Z | 2017 | 12 | 2017-12-27T18:06:48Z | 0 | 0 | 0900006482d77d30 |
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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;