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What are the IRB submission requirements for observational studies?
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Questions on regulations for process development and purchased human cells
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What training documentation is required for conducting clinical research studies?
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What are ethical considerations for a trial with a pre-study washout period?
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What are the IRB review requirements for web-based recruitment platforms?
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How to resolve irregularities in the documentation of informed consent?
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Can the IRB approve reimbursement of copays for routine costs in a clinical trial?
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Is IRB review required for survey results that may be published?
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