Regulatory
WCG Clinical | Insights
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
WCG Clinical | Insights
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
WCG Clinical | Insights
[Video] Institutional Biosafety Committee Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
WCG Clinical | Insights
IBC Review: Strategies to Secure Rapid IBC Approval for Human Gene Transfer Trials
Videos
WCG Clinical | Insights
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
WCG Clinical | Insights
The IRB’s Perspective: Determining Optimal Compensation for Clinical Trial Participants
Whitepapers
WCG Clinical | Insights
Toolbox Medical Relies on WCG IRB’s Prompt, Personalized Expertise in an Unsettled Environment
Case Studies
WCG Clinical | Insights
Is IRB review required when linking to clinicaltrials.gov postings on patient advocacy websites and newsletters?
Blog Posts
WCG Clinical | Insights
Save 456 Days in IRB Review With a Seamless, Coordinated Submission Process
Case Studies
WCG Clinical | Insights