Webinar On Risk Management in Clinical Trials
About This Event
This webinar will refresh basic Risk Management methodology and then establish how this fits in with the standard stages of a clinical trial. Regulatory inspectors will now expect to see evidence of a risk based approach to a clinical trial, and this course will address the topic of documentation to be created.
Areas Covered in the Session :
Risk management methodology
Utilize the basic principles to take a 'risk-based approach'
Document risks identified
Prioritise risks and plan mitigation actions where necessary
Who Will Benefit:
Data management Teams
Clinical Research Associates
Monitors
Project Managers
Statisticians
Academic Research Organizations' Staff
Representatives of any CROs or other contractors (ePRO etc) who will be supporting clinical trials
Researchers within a healthcare setting
And all clinical research professional embarking on a risk-based approach
For more information about this event please visit
https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1258