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Posted on October 25th, 2017
Compliance Oversight Determinations A. 7. Contingent Approval of Research with Substantive Changes and no Additional Review by the Convened IRB. A. 12. Failure to Conduct Continuing Review at Least Once per Year. F. 25. Failure to Document Informed Consent or of the IRB to Appropriately Waive the Requirement to Document Informed Consent. F. 26. Failure to Provide a Copy of the Informed Consent Document (ICD) to the Subject or the Subject's Legally Authorized Representative. F. 27. Inadequate ICD for Specific Research/Lack of Basic Elements.
Posted on October 29th, 2014
Posted on October 19th, 2014
Posted on October 16th, 2014
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