Overview
Course Description
- Clinical research fundamentals
- Research ethics and participant protection
- Informed consent
- Clinical study designs
- Bias, confounding and causality
- Statistics, validity, reliability and power
- Trial governance and documentation
- Safety and adverse events
- Trial lifecycle and close-out
- Knowledge-check questions
Course Content
2 Lectures • 2 hrs
Module 1
-
Introduction to the principles and practice of clinical research
Link to register with NIH IPPCR
-
Registeration for free
Includes
2 hrs on-demand video- 69 downloadable
resources
Full lifetime
access
Access on
mobile and TV
Assignments
Certificate
of Completion
Includes
Duration:
2 hrs
Chapters:
2
Video:2 hrs
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