Principal Investigator
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
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
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
Ethics in Clinical Research
Compensating Research Participants FAQ
Blog Posts