Regulatory
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
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
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
Cell & Gene Therapy
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers
Series: Ask the IRB & IBC Experts
Is informed consent needed for post-market patient registry?
Blog Posts
Diversity & Inclusion
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
Ethics in Clinical Research