Cardiology
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
Series: WCG Patient Forum
Fibromuscular Dysplasia Society of America: Collaboration Between Patients, Researchers, and Physicians Saves Lives
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
Protecting Patients, Protecting Your Study: The Benefits Of A Well-Run Data Monitoring Committee
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