Ethics, Compliance and Regulatory Guidance
CenterWatch | Insights
FDA Guidance Portal
Resource Hub
CenterWatch | Insights
The Basics of the Individual Expanded Access Request Process: A Resource for Physicians
Whitepapers
CenterWatch | Insights
Key Takeaways From FDA’s New Draft Guidance, “Studying Multiple Versions of a Cellular or Gene Therapy Product in an Early-Phase Clinical Trial”
Blog Posts
CenterWatch | Insights
More Than Good Intentions: DE&I Requires a Program-Level, Strategic Framework
Whitepapers
CenterWatch | Insights
Changes in Research: What are They and When do They Need to be Submitted to the IRB?
Whitepapers
CenterWatch | Insights
Do You Know Me?: The Subtle Distinction Between “Anonymous” and “De-identified” Data in Clinical Research
Whitepapers
CenterWatch | Insights
National and Local Coverage Determinations Every Coverage Analyst Should Know
Whitepapers
CenterWatch | Insights
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
CenterWatch | Insights
Compensating Research Participants FAQ
Blog Posts
CenterWatch | Insights