Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Clinical Endpoints
VRFCAT: Assessing Cognitive Function in Daily Living
Blog Posts
FDA & ICH
Do all subjects need to be reconsented with the revised consent form?
Blog Posts
Ethics in Clinical Research
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
FDA & ICH
Does my customer survey project require IRB review?
Blog Posts
COVID-19
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts
Protecting Patients, Protecting Your Study: The Benefits Of A Well-Run Data Monitoring Committee
Blog Posts
Participant Recruitment
Can you use patient Electronic Health Records to identify and recruit subjects?
Blog Posts
Site Efficiency
Using an IRB’s Site Relationships to Relieve “Site Crunch” and Reduce Trial Pressures
Blog Posts
Series: Ask the IRB & IBC Experts
Is informed consent needed for post-market patient registry?
Blog Posts
Clinical Trial Operations