Training Program Title
Risk-Based Monitoring Clinical Trials
CTSA Hub Administered
Contact us by email at firstname.lastname@example.org or by phone at 215-822-8644.
Training Program Description
Most site personnel have been exposed to the term risk based monitoring (RBM). But what is meant by RBM and where did the term come from? In addition to explaining the definition and rationale for RBM, this presentation will demonstrate how it will be implemented by clinical trial Sponsors and what the downstream effects will be to sites. Lastly, the presentation will provide insight into what sites need to do to best prepare for this new monitoring paradigm.
This is a 60 minute internet media player video of a voice over slide show.
A quiz concluding the presentation will summarize the topic and evaluate your understanding of the material.
Risk Based Monitoring (RBM)
Digital Commons Disciplines
Cost to Access
At the completion of the webinar, participants should be able to:
- Understand the rationale for changing the fundamentals of the clinical trial monitoring process
- Describe what is Risk Based Monitoring in Clinical Trials
- Recognize how Risk Base Monitoring will affect the clinical trial Site.
- Identify current Site processes that will need to be altered to accommodate clinical trials Risk Based Monitoring
Clinical Research Professionals (other than PI)