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Essentials of Clinical Trial Monitoring (G8)

Essentials of Clinical Trial Monitoring (G8)

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Who should attend?

This course is for all those involved in clinical research monitoring. It covers a wide range of topics and is designed for those who have been in the role for only a few months as well as the experienced CRA.

Details

This practical course defines the role of the clinical research monitor and explains the interaction with others in key roles as part of the clinical trial process as well as exploring the more complex aspects of clinical trial monitoring. Guidance will be given on best practices for selecting investigators, conducting monitoring visits and safety reporting. Delegates will explore strategies for dealing with common clinical trial management issues and how to adopt a preventative approach to handling monitoring issues. The course also summarises the essential documentation required during the clinical trial and gives an introduction to the key requirements of clinical trial project management. The course uses a blend of trainer input, exercises and delegate interaction.

Prices

Member 450 GBP, Non Member 550 GBP, Discounts for those working in the NHS or Academia

Contact

James Christianson
office@icr-global.org.uk

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