This refresher course is designed for clinical research professionals who have completed the foundational training, Ethics and Human Subject Protection: An Introduction with ICH E6(R3) Guidance.
Now updated to reflect the latest guidance from ICH E6(R3), this on-demand training is a must for clinical research professionals at any stage of their career—whether you’re just starting out or looking to reinforce your foundational knowledge.
This interactive, scenario-driven training course equips clinical research professionals with the skills to ensure informed consent is obtained from the right subject, using the correct forms, by authorized personnel, through a compliant process, at the appropriate time—with complete and accurate documentation.
Form FDA 1572 doesn’t have to be complicated. This practical training course equips sponsor personnel and site staff with the knowledge and tools to complete the Statement of Investigator accurately and confidently—right from the start.
This course provides a solid foundation to the key concepts and principles outlined in ICH GCP E6(R3). Through focused microlearning modules, real-world scenarios, and relevant knowledge checks, you’ll gain a deeper understanding of the guideline’s application in clinical trials to navigate the complexities of clinical research.