Overview
The Medidata Risk Management application allows study team members to identify, document, and monitor the risks of a study protocol and document activities within a Risk Plan Report. Risk Management supports the identification of Critical Data and Processes (Critical to Quality Factors), risk identification and evaluation, development of risk control strategies, cross-functional risk communication and review, and risk reporting. Risk Management also supports the capability to identify and track performance indicators, such as KRIs and QTLs, to assist with risk & mitigation oversight.
This course shows study end users of Risk Management how to generate new and access previous risk plan and QTL summary reports.
Recording of Global Education training sessions is strictly prohibited. Any attempts to record training will result in an immediate stoppage of training until recording is terminated.
Course Type
eLearning
Audience
Clinical Trial Administrators, Data Managers, Monitors, Reporting Specialists, Site/User Administrators
Duration
4 min
Languages
English
Product
Medidata Risk Management
Course Supplements
Course Outline - Generating Reports in Medidata Risk Management Outline - ENG