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Whitepapers
Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?
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What are IRB submission requirements for post marketing safety reports?
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May I pay a physician for referring a patient to our study?
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What is the IRB’s role in making the nonsignificant risk device determination?
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News & Events
WCG IRB Experts to Present at PRIM&R’s Advancing Ethical Research Conference
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Submitting protocol changes to the IRB prior to submitting to FDA
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Videos
Institutional Biosafety Committee Review for Genetically Modified Vaccines and Gene Transfer Products
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News & Events
WCG Announces the Formation of WCG IRB and the Launch of New WCG IRB Connexus™
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