documents: FDA-2000-N-0108-0073

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2000-N-0108-0073 FDA FDA-2000-N-0108 Reference 1. "Detailed Guidance on the Collection, Verification and Presentation of Adverse Reaction Reports Arising From Clinical Trials on Medicinal Products for Human Use" [Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products and Safety Reporting Requirements for Bioavailability and Bioequivalence Studies in Humans, Final Rule] Supporting & Related Material BKG-Background Material 2010-09-29T04:00:00Z 2010 9     2010-09-29T15:03:54Z   0 0 0900006480b62574

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