documents: FDA-1999-D-0081-0005

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1999-D-0081-0005 FDA FDA-1999-D-0081 Testing of Retroviral Vector-Based Human Gene Therapy Products for Replication Competent Retrovirus During Product Manufacture and Patient Follow-up Draft Guidance for Industry Other Guidance 2018-07-12T04:00:00Z 2018 7 2018-07-12T04:00:00Z   2024-11-07T01:33:38Z   1 0 09000064834dd664

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