Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Lessons Learned from 600+ Expert Committee Members
Blog Posts
Clinical Trial Operations
Preparing for Success: A Better Way to Manage the Feasibility Process
Blog Posts
Clinical Endpoints
How Calibrated Are Your Trial-Measurement Tools?
Blog Posts
Clinical Trial Safety
What are the IRB Reporting Requirements for Adverse Events?
Blog Posts
Clinical Trial Safety
Do we need to submit safety events from another site to our IRB?
Blog Posts
Cell & Gene Therapy
How should we handle financial conflicts of interest in FDA-regulated clinical trials?
Blog Posts
FDA & ICH
What are the signature requirements for translated informed consent documents?
Blog Posts
Series: Ask the IRB & IBC Experts
Can participants be reconsented over the phone when an ICF is updated?
Blog Posts
FDA & ICH
What are the IRB submission requirements for observational studies?
Blog Posts