Med/Sci
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
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
The IRB’s Perspective: Determining Optimal Compensation for Clinical Trial Participants
Whitepapers
COVID-19
Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
Case Studies
Participant Recruitment