Event Description
All staff currently working on CTIMPs must complete an ICH-GCP (6) R3 GCP Refresher by 28 April.
This course meets the GCP refresher requirements under ICH-GCP E6 (R3) and the new UK Clinical Trials Regulations which apply to all CTIMPs from this date.
Equivalent ICH-GCP E6 (R3) Refresher GCP courses are also acceptable (e.g. NIHR Good Clinical Practice (GCP) Refresher: GCP E6(R3)) .
If you are unsure if other courses meet these requirements, please contact the KHP-CTO Training Team for advice.
From April 2026, all Clinical Trials of Investigational Medicinal Products (CTIMPs) in the UK must operate in line with ICH-GCP E6 (R3) and the UK Clinical Trials Regulations (2025). These updates clarify expectations in areas such as:
- oversight
- risk-based approaches
- documentation
- transparency.
This course covers what has changed, what remains the same, and how the updated framework is intended to be applied in practice. It is intended to support staff in continuing their trial roles with confidence as the new regulatory framework takes effect.