Med/Sci
Clinical Trial Safety
WCG IRB Central and Institutional Site Relationships
Case Studies
New Applications, New Use Cases: The Expanding Need for Endpoint Adjudication
Whitepapers
Ethics in Clinical Research
Drafting a Research Plan for IRB Review and Research Conduct: Information That Must Be Included in a Clinical Trial Protocol
Whitepapers
Hybrid & Decentralized Trials
Complex Clinical Trial Protocol Designs: The Impact on Research Sites and the Role of a Central IRB
Blog Posts
Series: Ask the IRB & IBC Experts
Adults with Limited Capacity to Consent to Research
Blog Posts
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 Expert Endpoint Adjudication and Data Monitoring Committee Solutions Sell Sheet
Solution Overviews
Clinical Endpoints