This full day workshop runs four times a year and is appropriate for staff who need to be familiar with Good Clinical Practice (for research) and may need to be fully trained in the more rigorous requirements of a clinical trial of an investigational medicinal product (CTIMP). The course is aimed at those staff undertaking both low risk projects (e.g. studies using questionnaires only) and high risk projects such as drug trials. At the end of the course those attending should be able to:
- Appreciate the need for regulation of clinical research
- Understand the UK legislative framework for CTIMPs
- Be familiar with the principles & conditions of Good Clinical Practice
- Understand the practicalities of demonstrating GCP compliance.
Course places can be booked via Roy Halliday, Research & Development Support Officer, NHS Fife (email email@example.com).