One day workshop for monitoring clinical research in the NHS / Universities.

Who Should Attend

This workshop is designed for NHS / Academic staff whose role involves monitoring clinical research either governed by the ‘UK Policy Framework for Health & Social Care Research’ and/or governed by the regulations required for clinical trials of medicinal products or medical devices. For example monitors, research nurses, trial managers, project managers, R&D staff. Management staff involved with supervising monitors or managing oversight of research activity will find this workshop of interest.

Description

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:

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• Define the purpose and discuss the benefits of monitoring clinical research
• Plan and conduct a monitoring visit
• Ensure compliance to the research protocol and appropriate regulations
• Ensure patient safety
• Ensure data and essential documentation are accurate and in the appropriate format for sponsors, auditors and inspectors
• Record findings and the agreed actions in a monitoring report

 

As it is only 1 day pre reading is required prior to attendance.