documents: FDA-2024-N-5468-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2024-N-5468-0001 FDA FDA-2024-N-5468 Agency Information Collection Activities; Proposed Collection; Comment Request; Food and Drug Administration’s Adverse Event and Product Experience Reporting Program Notice 60 Day Proposed Information Collection 2025-01-17T05:00:00Z 2025 1 2025-01-17T05:00:00Z 2025-03-19T03:59:59Z 2025-03-22T01:00:51Z 2025-01149 0 0 09000064868e2fb4

Links from other tables