Update in Clinical Research & GCP        

Tuesday 16th June 2026 2 pm BST, 3 pm CET, 9am EDT (Boston).

Stay compliant and ahead of the curve in an evolving regulatory landscape while strengthening your understanding of global GCP standards. Join us for a comprehensive update in clinical research and GCP delivered as a three-hour webinar.  We will provide an overview of the latest updates in international guidelines and legislation shaping the future of clinical research.

Key highlights:

·        Recent revisions to ICH E6(R3), ICH E8(R1), ICH E19 and upcoming draft ICH guidance documents (ICH guidelines E20, E21, E22, E23)

·        Updated legislation and guidelines from the UK, EU and FDA

·        WHO Guidance for best practices for clinical trials 2024

·        Practical implications for sponsors, investigators, and research staff

The webinar is ideal for those involved in the design, set up, conduct, monitoring, auditing, and analysis of clinical trials involving medicinal products globally, including researchers, sponsors, CROs, consultants, healthcare professionals, clinical trial sites and R&D departments, service providers and RECs.

The course is designed to supplement knowledge of GCP and regulatory guidelines/legislation on clinical research. Prior basic knowledge of basic GCP is advised. The course will consist of presentations, poll questions, and followed by an online quiz.

Our normal webinar pricing applies:

• Individual connections (single participant): £200
• Single connection with up to 5 people taking part – note one connection only): £350
• Single connection with 5+ people taking part – note one connection only): £500
• Special rates available for organisations needing multiple connections - please contact us for details