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documents: FDA-2012-N-0921-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2012-N-0921-0001 FDA FDA-2012-N-0921 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Electronic Submission of Food and Drug Administration Adverse Event Reports and Other Safety Information Using the Electronic Submission Gateway and the Safety Reporting Portal Notice 60 Day Proposed Information Collection 2012-09-14T04:00:00Z 2012 9 2012-09-14T04:00:00Z 2012-11-14T04:59:59Z 2015-11-10T18:53:41Z 2012-22659 0 0 0900006481117417

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