Regulatory
WCG Clinical | Insights
Complex Clinical Trial Protocol Designs: The Impact on Research Sites and the Role of a Central IRB
Blog Posts
WCG Clinical | Insights
Live Survey Results – Part 4: Complex Clinical Trial Protocol Designs: The Effect on Research Sites and the Role Central IRBs Play in Ensuring Quality
Blog Posts
WCG Clinical | Insights
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
WCG Clinical | Insights
Does my customer survey project require IRB review?
Blog Posts
WCG Clinical | Insights
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts
WCG Clinical | Insights
Is informed consent needed for post-market patient registry?
Blog Posts
WCG Clinical | Insights
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
WCG Clinical | Insights
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
WCG Clinical | Insights
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts
WCG Clinical | Insights