Principal Investigator
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
Clinical Trial Agreement Language: Details in the Subject Injury Provision You Shouldn’t Overlook
Videos 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
Should You Be Adjudicating Your Clinical Endpoints?
Whitepapers WCG Clinical | Insights
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts WCG Clinical | Insights