documents
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
6 rows where docket_id = "FDA-2022-D-0588" 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 5
agency_id 1
- FDA 6
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2022-D-0588-0013 | FDA | None FDA-2022-D-0588 | Compliance Policy Regarding Blood and Blood Component Donation Suitability, Donor Eligibility and Source Plasma Quarantine Hold Requirements Guidance for Industry; Final Guidance | Other | Guidance | 2023-10-18T04:00:00Z | 2023 | 10 | 2023-10-18T04:00:00Z | 2025-11-06T10:00:05Z | 1 | 0 | 0900006486106c94 | ||
| FDA-2022-D-0588-0012 | FDA | None FDA-2022-D-0588 | Compliance Policy Regarding Blood and Blood Component Donation Suitability, Donor Eligibility and Source Plasma Quarantine Hold Requirements; Guidance for Industry; Availability. | Rule | Final Rule | 2023-10-18T04:00:00Z | 2023 | 10 | 2023-10-18T04:00:00Z | 2023-10-19T13:45:19Z | 2023-22957 | 0 | 0 | 090000648610438b | |
| FDA-2022-D-0588-0010 | FDA | None FDA-2022-D-0588 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice for Blood and Blood Components and Reducing the Risk of Transfusion-Transmitted Infections | Notice | 30 Day Proposed Information Collection | 2023-08-24T04:00:00Z | 2023 | 8 | 2023-08-24T04:00:00Z | 2023-09-26T03:59:59Z | 2023-09-26T01:01:03Z | 2023-18245 | 0 | 0 | 0900006485ee0a06 |
| FDA-2022-D-0588-0002 | FDA | None FDA-2022-D-0588 | Compliance Policy Regarding Blood and Blood Component Donation Suitability, Donor Eligibility and Source Plasma Quarantine Hold Requirements- Draft Guidance for Industry | Other | Guidance | 2022-05-24T04:00:00Z | 2022 | 5 | 2022-05-24T04:00:00Z | 2023-10-18T15:52:53Z | 0 | 0 | 09000064850def70 | ||
| FDA-2022-D-0588-0003 | FDA | None FDA-2022-D-0588 | Reference 1 Alternative Procedures for Blood and Blood Components During the COVID-19 Public Health Emergency | Supporting & Related Material | Background Material | 2022-05-24T04:00:00Z | 2022 | 5 | 2022-05-24T15:55:26Z | 0 | 0 | 09000064850df06b | |||
| FDA-2022-D-0588-0001 | FDA | None FDA-2022-D-0588 | Compliance Policy Regarding Blood and Blood Component Donation Suitability, Donor Eligibility and Source Plasma Quarantine Hold Requirements; Draft Guidance for Industry; Availability | Proposed Rule | Advance Notice of Proposed Rulemaking (ANPRM) | 2022-05-24T04:00:00Z | 2022 | 5 | 2022-05-24T04:00:00Z | 2022-07-26T03:59:59Z | 2023-10-18T18:54:08Z | 2022-11120 | 0 | 0 | 09000064850dbdae |
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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;