documents: FDA-2019-N-2175-0003

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-N-2175-0003 FDA FDA-2019-N-2175 Reference 1 - Flynn K.E, C.L. Hahn, J.M. Kramer, et al. (2013), “Using Central IRBs for Multicenter Clinical Trials in the United States,” PLOS ONE 8(1): e54999. RE Institutional Review Boards; Cooperative Research Supporting & Related Material Background Material 2022-09-28T04:00:00Z 2022 9     2022-09-28T19:18:31Z   0 0 0900006485379fd7

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