Oncology
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
Does the IRB need to approve doctor-to-doctor letters?
Blog Posts
Regulatory Compliance
What are the IRB review requirements for human factors/usability testing?
Blog Posts
Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Clinical Endpoints