Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
WCG Clinical | Insights
Preparing for Success: A Better Way to Manage the Feasibility Process
Blog Posts
WCG Clinical | Insights
How Calibrated Are Your Trial-Measurement Tools?
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
How should we handle financial conflicts of interest in FDA-regulated clinical trials?
Blog Posts
WCG Clinical | Insights
What are the signature requirements for translated informed consent documents?
Blog Posts
WCG Clinical | Insights
Can participants be reconsented over the phone when an ICF is updated?
Blog Posts
WCG Clinical | Insights
What are the IRB submission requirements for observational studies?
Blog Posts
WCG Clinical | Insights
Questions on regulations for process development and purchased human cells
Blog Posts
WCG Clinical | Insights