Biotech Leaders
AIMS User Guide
Solution Overviews
Ethics in Clinical Research
Ask the Experts: When Do I Report a Protocol Deviation to the IRB? Do I Need To Report a Summary of Deviations at the Time of Continuing Review?
Blog Posts
FDA & ICH
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
Clinical Endpoints
WCG Supports Small Oncology Biotech Through Rapid Growth, Saving Hundreds of Thousands of Dollars
Case Studies
Participant Recruitment
WCG Support Lifts Study Enrollment by 56%
Case Studies
Cell & Gene Therapy
[Video] Institutional Biosafety Committee Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
IBC Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
Clinical Endpoints
See How WCG Helped a Mid-tier Biopharma Respond to an Urgent FDA Request, and Adjudicated 400 Endpoints in Just a Few Short Weeks
Case Studies
Ethics in Clinical Research
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
Ethics in Clinical Research