About this course

After completing this course, you will be able to:

  • Describe types of data and the principles of data collecting and management in clinical trials.
  • Outline the principles and key elements of overall clinical trial quality management and the stakeholders involved.
Investigator Brochure | Patient Reported Outcomes (PROs) | E-Patient Reported Outcomes
Duration: 4 hours
Recommended Courses: 21

Dates

Start date: 13/08/20

Course files