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January 27, 1981\" - [Informed Consent Elements; Final Rule]", "Supporting & Related Material", "BKG-Background Material", "2011-01-04T05:00:00Z", 2011, 1, null, null, "2011-06-11T16:28:12Z", null, 0, 0, "0900006480bc1ee7"], ["FDA-2009-N-0592-0072", "FDA", "FDA-2009-N-0592", "Reference 2 - \"The Belmont Report..., April 18, 1979\" - [Informed Consent Elements; Final Rule]", "Supporting & Related Material", "BKG-Background Material", "2011-01-04T05:00:00Z", 2011, 1, null, null, "2011-06-11T16:28:12Z", null, 0, 0, "0900006480bc1ee9"], ["FDA-2009-N-0592-0080", "FDA", "FDA-2009-N-0592", "Reference 9e - \"Informed Consent to Participate in Research, University of Texas at Austin\" - [Informed Consent Elements; Final Rule]", "Supporting & Related Material", "BKG-Background Material", "2011-01-04T05:00:00Z", 2011, 1, null, null, "2011-06-11T16:28:16Z", null, 0, 0, "0900006480bc2094"], ["FDA-2009-N-0592-0089", "FDA", "FDA-2009-N-0592", "Reference 15 - \"Guidance for Sponsors, Institutional Review Boards, Clinical Investigators and FDA Staff: Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens That Are Not Individually Identifiable, April 25, 2006\" - [Informed Consent Elements; 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