Research Sponsors
Reinventing Site Feasibility
Videos
AIMS User Guide
Solution Overviews
WCG Helps Sponsor Secure 200 Investigators in 5 Days
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
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
Relieving the Safety Reporting Burden on Sites: 4 Takeaways
Articles
Clinical Endpoints