Regulatory Compliance
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Diversity & Inclusion
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
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Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
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Participant Recruitment
Does the IRB need to approve doctor-to-doctor letters?
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Regulatory Compliance
What are the IRB review requirements for human factors/usability testing?
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Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
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FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
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Ethics in Clinical Research
Compensating Research Participants FAQ
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Ethics in Clinical Research
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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FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
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Ethics in Clinical Research