Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Leveraging Standardized Data to Streamline Site Feasibility
Blog Posts
Ethics in Clinical Research
The FDA’s Guidance on Electronic Records and Signatures: Key Takeaways
Blog Posts
Artificial Intelligence and Machine Learning in Clinical Trials
The Role of AI in Regulatory Decision-Making for Drugs & Biologics: the FDA’s Latest Guidance
Blog Posts
Site Complexities and Start-up Barriers in Clinical Trials
Blog Posts
Ethics in Clinical Research
The FDA Accepts ICH E11A on Pediatric Extrapolation: How Does This Impact Your Pediatric Study?
Blog Posts
Biosafety
What Is a Biological Safety Cabinet? Do We Need One to Prepare Our Gene Therapy Product?
Blog Posts
Streamlining Recruitment & Retention with ClinSphere™ Total Enrollment
Blog Posts
Ethics in Clinical Research
How Do PIs Report PRI in a Blinded Study Without Unblinding Themselves?
Blog Posts
Diversity in Clinical Trials
Diversity in Clinical Research: Every Participant Counts
Blog Posts
Diversity in Clinical Trials