Participants will be looking at the risk adapted approaches to the monitoring of clinical research studies and trials.

Please note the other workshop 'Monitoring Non-Commercial Clinical Research Studies' goes into more detail of monitoring, particularly on-site monitoring visits. This workshop entails the risk adapted approaches. Please ensure you register for the correct session.

 

Who Should Attend

This workshop is designed for clinical research professionals for example sponsors , R&D Staff, Investigators, Trial Managers, Monitors, Research Nurses, Project Managers and Quality Assurance Staff. Management staff involved with supervising or managing oversight of research activity will find this workshop of interest.

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It will be an interactive day with a combination of presentations, discussions and workshop. By the end of this workshop, participants will be able to:​​

• State 6 examples of risk in clinical research studies
• Conduct a risk assessment of a clinical research study
• Identify appropriate monitoring approaches
• Develop a monitoring plan with the risk adapted approaches

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As it is only 1 day pre reading is required prior to attendance. Post course documents and useful templates and links are also emailed after the workshop