The notion and definition of what “Risk” is in the context of Clinical Trials is a topic that may change in the blink of an eye, but preventing and mitigating risks is still one of the most important tasks when it comes to Clinical Research. It leads to better results, less errors and more effective treatments, while simultaneously being extremely cost-efficient and time-saving. That is why we are organizing this Clinical Trails Risk Management Webinar for all that wish to keep up with the trends in the industry and produce better results in their professional endeavours.
Date: 8th May, 2015
Early-Bird Registration available until: 1st May, 2015
Who would benefit:
- Clinical Investigators
- CRAs/Monitors
- Clinical Trial Managers
- Sponsors
- Compliance specialists
- Regulatory Affairs professionals
- Students and academic staff
- Risk Management Staff
Training Agenda:
- What is risk management and is it worth the effort?
- Regulatory background to risk management – ICH Q9
- Basic principles of risk management
- Utilising risk management methodology in a clinical trial including usual risk triggers
- How to get started
- Documenting risks
- Identifying mitigating actions and managing them
- Risk management when CROs and/or other contractors are involved
- What next?
- DB Lock
