Reporting Insights

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What are the requirements for notifications of study closure at research sites?

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Changes in Research: What are They and When do They Need to be Submitted to the IRB?

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[Webinar] Do I Need to Submit THIS to the IRB? A Discussion of Changes in Research and Other Reportable (and Non-Reportable) Events

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How do I handle a deviation in the use of blood specimens collected outside the timeframe?

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How should a site document a missing signature on a HIPAA authorization form?

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Do we need to submit safety events from another site to our IRB?

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How to resolve irregularities in the documentation of informed consent?

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