Module Summary
CONTENT
Learning outcomes
CONTENT
Learning objectives
At the end of the course, the participant can:
- Explain how to conduct a clinical trial
- Explain the roles and responsibilities of the investigator and site staff, the tools and documents needed and how to track and keep records during the course of the study
- Describe the informed consent process and the management of subjects’ safety and safety reporting
- Describe the process to handle, store and document the study medication and medical devices