clinical trials

Learn how clinical trial sites are selected, initiated, monitored, and closed. Focus on GCP-compliant site operations, subject recruitment, and monitoring reports.

This intermediate-to-advanced course offers in-depth training on clinical trial operations, project management, and regulatory compliance. Learn how to handle site selection, budget planning, trial documentation, RBM, and audit readiness — skills essential for clinical trial leads and professionals.

This foundational course offers a comprehensive overview of how clinical trials are designed, conducted, monitored, and regulated. It’s perfect for beginners entering the world of medical research and clinical development.

Understand the global regulatory framework for clinical trials, including FDA submissions, ICH-GCP guidelines, IND/NDA applications, and post-marketing surveillance.