Biotech Leaders
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
The Role of IRBs in Research Oversight: Information for Research Teams to Support Diverse Research Participation
Whitepapers
Ethics in Clinical Research
The Role of IRBs in Research Oversight: Information for Potential Participants in Clinical Research
Whitepapers
Should You Be Adjudicating Your Clinical Endpoints?
Whitepapers
Clinical Endpoints
NASH Knowledge Forum: Evolving Industry Best Practices and Trends for Endpoint Adjudication and Imaging in NASH Trials
Videos
Clinical Endpoints
The Top 5 Benefits of Outsourcing Expert Committee Management to an Independent Provider
Whitepapers
Participant Recruitment