Oncology
Ethics in Clinical Research
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
The Great Resignation: Its Impact on Clinical Research & Where We Go From Here – Part 1
Blog Posts
Series: The Future of Clinical Research Sites
Complex Clinical Trial Protocol Designs: The Effect on Research Sites and the Role Central IRBs Play in Ensuring Quality
Videos
Expert Endpoint Adjudication and Data Monitoring Committee Solutions Sell Sheet
Solution Overviews
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
Cell & Gene Therapy