Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
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Clinical Endpoints
Common Challenges in Endpoint Assessment Training
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7 Key Considerations for Research Sites Contemplating Switching Their CTMS
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Clinical Endpoints
VRFCAT: Assessing Cognitive Function in Daily Living
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FDA & ICH
Do all subjects need to be reconsented with the revised consent form?
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Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
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FDA & ICH
Does my customer survey project require IRB review?
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COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
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Protecting Patients, Protecting Your Study: The Benefits Of A Well-Run Data Monitoring Committee
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Participant Recruitment
Can you use patient Electronic Health Records to identify and recruit subjects?
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Site Efficiency