documents: FDA-1999-D-0081-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0081-0002 FDA FDA-1999-D-0081 "Guidance for Industry: Supplemental Guidance on Testing for Replication Competent Retrovirus in Retroviral Vector Based Gene Therapy Products and During Follow-up of Patients in Clinical Trials Using Retroviral Vectors;" Availability Notice Notice of Data Availability 2000-10-24T04:00:00Z 2000 10     2025-07-01T21:48:06Z 00-26670 0 0 09000064804a6961

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