dockets: FDA-2005-D-0027

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

This data as json

id agency_id title docket_type last_modified object_id
FDA-2005-D-0027 FDA Guidance for Industry and Food and Drug Administration: Procedures for Handling Post-Approval Studies Imposed by PMA Order Nonrulemaking 2022-10-07T15:14:10Z 0b0000648043e82c

Links from other tables