documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
7 rows where docket_id = "FDA-2021-N-1333" and posted_year = 2024 sorted by posted_date descending
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Suggested facets: subtype, posted_date (date), comment_start_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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2021-N-1333-0028 | FDA | None FDA-2021-N-1333 | Reference 3--Medical Gas CPGM | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:17Z | 0 | 0 | 09000064865bd76c | |||
| FDA-2021-N-1333-0031 | FDA | None FDA-2021-N-1333 | Reference 6--FRIA Medical Gases | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:39Z | 0 | 0 | 09000064865bd771 | |||
| FDA-2021-N-1333-0025 | FDA | None FDA-2021-N-1333 | Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases | Rule | Final Rule | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T04:00:00Z | 2024-06-20T12:33:21Z | 2024-13190 | 0 | 0 | 09000064865bc84f | |
| FDA-2021-N-1333-0027 | FDA | None FDA-2021-N-1333 | Reference 2--Med Gas - Container Closure - OMQ White Paper | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:14Z | 0 | 0 | 09000064865bd76b | |||
| FDA-2021-N-1333-0026 | FDA | None FDA-2021-N-1333 | Reference 1--Certification Process Draft Guidance | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:11Z | 0 | 0 | 09000064865bd76a | |||
| FDA-2021-N-1333-0029 | FDA | None FDA-2021-N-1333 | Reference 4--Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:22Z | 0 | 0 | 09000064865bd76f | |||
| FDA-2021-N-1333-0030 | FDA | None FDA-2021-N-1333 | Reference 5--Postmarketing Safety Reporting Draft Guidance | Supporting & Related Material | Background Material | 2024-06-18T04:00:00Z | 2024 | 6 | 2024-06-18T15:24:36Z | 0 | 0 | 09000064865bd770 |
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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;