This interactive simulation-powered training program helps ensure compliance with international standards for Good Clinical Practice ICH E6(R2) in clinical trials.
This interactive, simulation-powered training program helps ensure informed consent is obtained by the right subject, with the right forms, by the right people, through the right process, at the right time, and with the right documentation.
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.