CROs
What is the IRB’s responsibility for the review of updated Investigator Brochures?
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Ethics in Clinical Research
If a Subject’s Care Is Divided Equally Between Two Caregivers, Who Should Sign Caregiver Consent?
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Is it ethical to pay subjects for referring friends to a clinical research site?
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Regulatory Compliance
How should a site document a missing signature on a HIPAA authorization form?
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Live Q&A on Reducing Placebo Response & Measurement Error
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Lessons Learned from 600+ Expert Committee Members
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Clinical Trial Operations
Preparing for Success: A Better Way to Manage the Feasibility Process
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Placebo Response Reduction
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Clinical Trial Safety
What are the IRB Reporting Requirements for Adverse Events?
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Clinical Trial Safety