Citations are generated automatically from bibliographic data as a convenience and may not be complete or accurate.
Food and Drug Administration, Health and Human Services Department. "Draft Guidance for Hde Holders, Institutional Review Boards (Irbs), Clinical Investigators, and FDA Staff: Humanitarian Device Exemption Regulation, Questions and Answers". Government. Health and Human Services Department, January 1, 2008. https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS111189
Food and Drug Administration, Health and Human Services Department. (2008, January 1). Draft Guidance for Hde Holders, Institutional Review Boards (Irbs), Clinical Investigators, and FDA Staff: Humanitarian Device Exemption Regulation, Questions and Answers. [Government]. Health and Human Services Department. https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS111189
Food and Drug Administration, Health and Human Services Department. Draft Guidance for Hde Holders, Institutional Review Boards (Irbs), Clinical Investigators, and FDA Staff: Humanitarian Device Exemption Regulation, Questions and Answers. Health and Human Services Department, (1 Jan 2008), https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS111189
Food and Drug Administration, Health and Human Services Department, Draft Guidance for Hde Holders, Institutional Review Boards (Irbs), Clinical Investigators, and FDA Staff, GovInfo, (January 1, 2008), https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS111189