The UK Clinical Trial Regulations

Recordinmg of the webinar from Tuesday 14th April 2026

This webinar is ideal for those involved in the set up and conduct of clinical trials involving medicinal products in the UK, including researchers, sponsors, CROs, consultants, healthcare professionals, clinical trial sites and R&D departments, service providers and RECs.
Prior knowledge of basic GCP is advised.

The webinar consisted of presentations, poll questions, and followed by an online quiz and there will be the opportunity to ask questions

Following Brexit, an update to the UK Medicines for Human Use (Clinical Trials) Regulations 2004 took place on April 2025 and the new UK CTR 2025 will come into force on 28^th April 2026. This webinar will be delivered as a two-hour webinar and will cover the regulation, new terminology and supporting guidance’s from the MHRA and HRA. 
The new legislation will also implement the latest international Good Clinical Practice (GCP) guidelines (ICH-GCP E6(R3)).  However, these guidelines will not be included in this webinar as they are covered in a separate webinar.

A certificate will be provided for each participant who completes the webinar recording