documents: FDA-2019-D-2330-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2019-D-2330-0001 FDA FDA-2019-D-2330 Pathology Peer Review in Nonclinical Toxicology Studies: Questions and Answers; Draft Guidance for Industry; Availability Notice Notice of Availability 2019-08-01T04:00:00Z 2019 8 2019-08-01T04:00:00Z 2019-10-01T03:59:59Z 2019-10-05T01:04:09Z 2019-16361 0 0 0900006483dddb19

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