Musculoskeletal
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
Whitepapers
Complex Clinical Trial Protocol Designs: The Impact on Research Sites and the Role of a Central IRB
Blog Posts
Adults with Limited Capacity to Consent to Research
Blog Posts
What are the requirements for notifications of study closure at research sites?
Blog Posts
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
Complex Clinical Trial Protocol Designs: The Effect on Research Sites and the Role Central IRBs Play in Ensuring Quality
Videos
Can a protocol get IRB approval during the 30-day IND waiting period?
Blog Posts
Does my customer survey project require IRB review?
Blog Posts
WCG IRB’s Single-Patient Expanded Access Experience Before and During the COVID-19 Pandemic
Blog Posts