Clinical Trial Safety

Clinical Endpoints
See How WCG Helped a Mid-tier Biopharma Respond to an Urgent FDA Request, and Adjudicate 400 Endpoints in Just a Few Short Weeks
Case Studies
Clinical Endpoints
The Burden of Safety Reporting on Sites: An Oncology Site’s Perspective
Videos
Cell & Gene Therapy
Four Key Elements You Need to Know About the Role of IBCs in Gene Therapy Trials
Blog Posts
Cell & Gene Therapy
As a sponsor, does my HGT clinical trial require IBC approval at all sites?
Blog Posts
Cell & Gene Therapy
Does Human Gene Transfer research at my site require IBC approval?
Blog Posts
Clinical Trial Safety
What are IRB submission requirements for post marketing safety reports?
Blog Posts
Clinical Endpoints
How WCG Statistics Collaborative Helped Breakthrough Therapy Obtain Regulatory Approval
Case Studies
Clinical Trial Safety
Submitting Deviations from a Sponsor’s Adverse Event Reporting Requirements to the IRB
Blog Posts
Clinical Endpoints
New Normal or Not, Safety Reporting Matters
Blog Posts
Clinical Endpoints