Research Sites & Institutions
Ethics in Clinical Research
Compensating Research Participants FAQ
Blog Posts
Ideal Vs. Reality: How to Create and Negotiate the Best Possible Clinical Trial Budget for Your Site
Videos
WCG Velos eResearch Case Study – Cancer Center
Case Studies
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
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