documents: FDA-2025-D-4634-0001
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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| FDA-2025-D-4634-0001 | FDA | FDA-2025-D-4634 | Monoclonal Antibodies: Streamlined Nonclinical Safety Studies; Draft Guidance for Industry; Availability | Notice | Notice of Availability | 2025-12-03T05:00:00Z | 2025 | 12 | 2025-12-03T05:00:00Z | 2025-12-03T19:23:31Z | 2025-21864 | 0 | 0 | 09000064b90abea8 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref