documents: FDA-2011-D-0514-0026

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

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-D-0514-0026 FDA FDA-2011-D-0514 Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act; Guidance for Industry and Food and Drug Administration Staff; and Procedures for Handling Post-Approval Studies Imposed by Premarket Approval Application Order; Guidance for Industry and Food and Drug Administration Staff; Availability - Final Guidance Notice Notice of Availability 2022-10-07T04:00:00Z 2022 10 2022-10-07T04:00:00Z   2022-10-07T16:19:27Z 2022-21832 0 0 09000064853d455b

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