Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Biosafety
Best Practices for Protecting Non-Participants in Human Gene Transfer Clinical Trials
Blog Posts
Ethics in Clinical Research
Regulatory Evaluations of Companion Diagnostic Medical Devices in Clinical Trials: Experiences of an Independent IRB
Blog Posts
Regulatory Compliance
ICH E6(R3) Readiness Assessment
Blog Posts
Pioneering Ethical Oversight in AI-Enabled Clinical Research: Insights on the New Framework
Blog Posts
Overcoming Study Start-up Delays: Best Practices for Research Sites
Blog Posts
Series: Ask the IRB & IBC Experts
What Is the Accelerated Approval Pathway? Understanding the Latest FDA Guidance
Blog Posts
Review of the FDA Draft Guidance: Considerations for Including Tissue Biopsies in Clinical Trials
Blog Posts
Artificial Intelligence and Machine Learning in Clinical Trials
Advancing Clinical Trials with AI
Blog Posts
Leveraging Standardized Data to Streamline Site Feasibility
Blog Posts
Ethics in Clinical Research