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Risk Management in Clinical Trials 2015
05 Oct 2015
Webinar
Home
Risk Management in Clinical Trials 2015
Description
Topics
Utilize the basic principles to take a `risk-based approach`
Risk management methodology
Prioritise risks and plan mitigation actions where necessary
Document risks identified
Who should Attend
Clinical Research Associates
Data management Teams
Project Managers
Monitors
Academic Research Organizations` Staff
Statisticians
Researchers within a healthcare setting
Representatives of any CROs or other contractors (ePRO etc) who will be supporting clinical trials
And all clinical research professional embarking on a risk-based approach
Past Events
Risk Management in Clinical Trials 2015 - 05 Oct 2015, Webinar
(54087)
Important
Please, check "Risk Management in Clinical Trials" official website for possible changes, before making any traveling arrangements
Event Categories
Business:
Quality assurance, Risk Management
Government & Global Issues:
Law & Regulations
Health & Medicine:
Medical device, Medical laboratories, Pharma
Science:
Biochemistry, Life Sciences & Biology
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