documents: FDA-1980-N-0049-0070

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1980-N-0049-0070 FDA FDA-1980-N-0049 Reference 10: "Guidance for Industry: How to Complete the Vaccine Adverse Event Reporting System Form (VAERS-1)," September 1998, http://www.fda.gov/cber/gdlns/vaers-1.pdf Supporting & Related Material Background Material 2003-12-29T05:00:00Z 2003 12     2020-05-19T17:17:27Z   0 0 09000064805b99ce

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