Research Sponsors
What elements of Informed Consent must we include when pre-screening?
Blog Posts
Clinical Endpoints
The Role of Expert Committees: An Interview with Dr. Seltzer
Videos
Ethics in Clinical Research
Does the IRB need to review news stories?
Blog Posts
Protecting Sponsors Against Bias and Variability
Articles
Single-Patient Expanded Access: WIRB experience in 2018
Blog Posts
How a Sponsor Secured 200 High-Performing PI’s in a New TA in Just 5 Days
Case Studies
Recommendations for Study Sponsors on Informed Consent Documents
Whitepapers
Limited IRB Review: Are You Prepared for January 21st?
Blog Posts
Site Efficiency
IRBs can make the most of central IRB partnerships
Articles
Clinical Trial Safety