Common Rule Insights

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What Can Institutions with Local IRBs Do to Prepare for a Proposed FDA Single IRB Mandate?

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Reviewing the FDA’s Proposed Single IRB Mandate

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Reviewing the FDA’s Proposed Informed Consent Rule Changes

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Does my customer survey project require IRB review?

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Have WCG IRBs adopted the 2018 revisions to the Common Rule for the Protection of Human Subjects?

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Does the Common Rule apply to Medicare-covered investigational device studies?

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