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SACHRP January 31, 2008 SACHRP letter to HHS Secretary_ Recommendatio _ HHS.gov.pdfSACHRP August 5, 2011 SACHRP Letter to the HHS Secretary 3 _ HHS.gov.pdfSACHRP Attachment D_ Informed Consent and Waiver of Consent _ HHS.gov.pdfSACHRP Attachment D_ FAQ's Terms and Recommendations on Informed Consent _ HHS.gov.pdfSACHRP Attachment D - Recommendations for a Broad Consent Template _ HHS.gov.pdfSACHRP Attachment C_ SACHRP Comments on FDA draft guidance “Use _ HHS.gov.pdfSACHRP Attachment C -New _Key Information_ Informed Consent Requirements _ HHS.gov.pdfSACHRP Attachment C - Updated FAQs Informed Consent for Use of Biospe _ HHS.gov.pdfSACHRP Attachment C - Recommendations for Broad Consent Guidance _ HHS.gov.pdfSACHRP Attachment A2 - Reconsent Appendix 2 _ HHS.gov.pdfSACHRP Attachment A1 - Reconsent Appendix 1 _ HHS.gov.pdfSACHRP Attachment A_ SACHRP Commentary on the FDA Draft Guidance _ HHS.gov.pdfSACHRP Attachment A_ Minimal Risk Informed Consent Models _ HHS.gov.pdfSACHRP Attachment A_ FAQs, Terms and Recommend. on Informed Consent _ HHS.gov.pdfSACHRP Attachment A - FAQs Relating to Recommendations on Broad Consent _ HHS.gov.pdfPage updated
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