WEBINAR

Mastering the
EU CTR

This educational webinar focused on helping clinical research professionals navigate the European Union Clinical Trials Regulation (EU CTR) and successfully align teams with the evolving regulatory framework.

Why It Matters:

As organizations continue expanding global clinical development programs, understanding EU CTR requirements is critical for regulatory compliance, submission efficiency, and successful trial execution across Europe.

Key Learning Objectives:

Understand the key differences between EU CTR and previous directives

Learn practical steps to ensure compliance across the trial lifecycle

Explore strategies for streamlining submissions through CTIS

Improve operational readiness for global clinical trials

Speakers

Jay Russak

Senior Director of Clinical Operations

Experienced clinical operations leader with a focus on operational excellence and patient-centric trial delivery.

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