Regulatory Compliance
WCG Clinical | Insights
What documentation needs to be submitted to the IRB for an IND exemption request?
Blog Posts
WCG Clinical | Insights
Does research involving retrospective review of patient charts require IRB review?
Blog Posts
WCG Clinical | Insights
Save 456 Days in IRB Review With a Seamless, Coordinated Submission Process
Case Studies
WCG Clinical | Insights
What are IRB submission requirements for post marketing safety reports?
Blog Posts
WCG Clinical | Insights
Guidance on genomic research with deceased patients
Blog Posts
WCG Clinical | Insights
Can we charge a subject for a diagnostic test not done as part of the IRB approved protocol?
Blog Posts
WCG Clinical | Insights
How should a site document a missing signature on a HIPAA authorization form?
Blog Posts
WCG Clinical | Insights
What are the IRB Reporting Requirements for Adverse Events?
Blog Posts
WCG Clinical | Insights
Do we need to submit safety events from another site to our IRB?
Blog Posts
WCG Clinical | Insights