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If My Study Includes Approved Drugs, When Do the Risks of Those Drugs Need to Be Disclosed in the Consent Form?
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Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
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The Collaboration of a Researcher With Breakthrough Science and a Patient In Need of Life Saving Medicine That Might Result
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Part 2: The Necessary Changes that Sites, Institutions and Research Participants are Considering During the COVID-19 Crisis
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WCG IRB Connexus™ Terms of Use Agreement
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