This one-day workshop follows on nicely from the ‘Monitoring Non-Commercial Clinical Research Studies’ and the ‘Risk Based Monitoring workshops. This workshop will go into more depth of monitoring
Investigational Medicinal Products (IMP) in pharmacy and clinical trial samples in the labs.​

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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:

• Define the purpose of monitoring clinical trials.

• Understand the role of pharmacy & labs in clinical trials.

• Plan and conduct Investigational Medicinal product (IMP) monitoring in Pharmacy.

• Ensure IMP are managed and dispensed to patients in accordance with the protocol.

• Monitor the system of controls governing the collection, processing, and storage of samples to ensure sample integrity and accurate results.

• Manage non-compliance(s)

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Who Should Attend​

This workshop is designed for NHS/ Academic staff whose role involves monitoring clinical research governed by the regulations required for clinical trials of medicinal products. For example, monitors, research nurses, trial managers, project managers, pharmacy staff, R&D staff. Management staff involved with supervising monitors or managing oversight of research activity will also find this course of interest.

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