Washington, DC: Food and Drug Administration [FDA], 2010 January 13: ? p. [Online]. Accessed: http://www.regulations.gov [2010 February 15]
United States. Food and Drug Administration [FDA]
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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 Center for Biologics Evaluation and Research [CBER] (United States) (2001-02-10)