Pharma: Clinical

A two-day course that will ensure you comply with new regulatory requirements.

This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the new EU Clinical Trial Regulation and a brief review of key FDA requirements.

This course provides the latest updates on the finalised ICH GCP E6 R3 guideline, EU Clinical Trial Regulation update, other EU and FDA requirements, consideration for managing studies in the future and AI and other technology developments.

Optimising oversight for inspection compliance.

This highly interactive and practical one-day course will introduce you to both the principles of GCP and give you an understanding of how to practically apply it in different settings.

Get clear, actionable guidance on E6(R3) requirements for digital tools, AI, risk-based approaches, and quality-by-design. Learn how to apply them to trial conduct, oversight, and regulatory readiness using real-world examples.

This course examines the MENA region’s growing role in clinical trials, driven by its diverse population, rising chronic disease rates, and supportive regulatory environment.