Research Sites & Institutions
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
Five Tips for Improving Your Site’s Study Start-Up Timelines
Blog Posts
Run Your Site Like a Business – A Framework for Success
Whitepapers
Clinical Trial Safety
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
Ideal vs. Reality Budgeting – Create & Negotiate the Best Clinical Trial Budget for Your Site
Whitepapers
Clinical Endpoints
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers Five Tips for Creating & Negotiating the Best Clinical Trial Budget for Your Site
Blog Posts
FDA & ICH