Become an expert on quality and risk-management strategies and procedures. This interactive eLearning course answers the fundamental questions: What is RBM and how is it different from the standard monitoring approach?
When in need of a comprehensive refresher, this on-demand eLearning course provides a consolidated overview on the history and importance of ethical conduct in clinical trials involving human subjects.
Learn the various responsibilities of clinical investigators based on FDA Regulations, ICH Guidance Documents, and international standards.
This course builds on foundational knowledge and provides practical, hands-on learning based on real-world scenarios, giving employers confidence that investigators are properly equipped to navigate problem resolution and risk mitigation.
Improve your consent process by learning how to assess a participant’s reading level, health literacy, and overall understanding of clinical trial participation and address culture, learning styles, emotional states and language. This eLearning course will provide essential tools for those directly involved in informed consent discussions.