Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
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
What training documentation is required for conducting clinical research studies?
Blog Posts
WCG Clinical | Insights
What are ethical considerations for a trial with a pre-study washout period?
Blog Posts
WCG Clinical | Insights
Get under the hood while the trial is running: Identify and rectify data problems before it’s too late
Blog Posts
WCG Clinical | Insights