Training Courses

For staff and students working on (or expecting to work or on) Clinical Trials of Investigational Medicinal Products (CTIMPs/drug trials). Covers GCP principles and the UK Medicines for Human Use (Clinical Trials) Regulations.

All CTIMP researchers must refresh every two years. This session is for those who have previously completed GCP training within the past 2 years and need to update their knowledge. Recommended for anyone with prior GCP training now due for renewal.

For those working only on studies that do NOT involve Investigational Medicinal Products (e.g. surgical or procedural studies). Focuses on applying GCP standards to non-drug research.

For staff or students analysing or processing trial samples. Emphasises data integrity, sample handling, and laboratory responsibilities under GCP. Recommended for laboratory staff working with trial material.

For pharmacy teams handling clinical trial products or supporting trial patients. Combines GCP principles with responsibilities specific to pharmacy practice. Recommended for pharmacy staff with trial responsibilities.

For staff who are not actively involved in a clinical trial, but may come into contact with trial participants during their normal duties (e.g. ward staff). Provides a concise introduction to GCP principles. Available at request.

For staff responsible for, or delegated to carry out, the archiving of clinical trial material. Covers the legal, regulatory, and practical requirements for long-term data storage.