Research Sites & Institutions
Five Tips for Creating & Negotiating the Best Clinical Trial Budget for Your Site
Blog Posts
FDA & ICH
Can a physician submit a single humanitarian use device (HUD) submission to the IRB?
Blog Posts
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