CROs
Series: The Future of Clinical Research Sites
The Great Resignation: Its Impact on Clinical Research & Where We Go from Here
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
WCG Imaging Solution Overview
Solution Overviews
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
Ethics in Clinical Research
FDA Guidance Portal
Resource Hub
Site Efficiency
Using an IRB’s Site Relationships to Relieve “Site Crunch” and Reduce Trial Pressures
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