This Webinar is now archived in our Insights page and is available on our YouTube Channel

Navigating the Impact of New EU Regulations (EU-CTR)

Date:  Wednesday, June 21st

Time:  1:00 PM EST / 10:00 AM PST

Webinar Overview

The EU Clinical Trial Regulation (EU-CTR) and Clinical Trials Information System (CTIS) have revolutionized the regulatory landscape and significantly impacted how sponsors manage electronic trial master files (eTMF) and regulatory information management (RIM) systems. With these changes come difficulties and complexities that require organizations to be prepared to navigate them effectively.

In this informative webinar, we will delve into the key changes and challenges in the EU regulatory landscape concerning eTMF and RIM systems to help ensure regulatory compliance and successful clinical trials.

By attending this webinar, you will:

• Gain a better understanding of the EU-CTR & CTIS regulations and their impact on eTMF and RIM systems.
• Learn about the challenges and complexities that come with these regulations.
• Discover best practices for optimizing your eTMF and RIM systems for regulatory compliance.
• Acquire actionable steps to ensure compliance with EU-CTR & CTIS regulations.

About Astrix

Astrix partners with many of the industry leaders in the informatics space to offer state of the art solutions for all of your laboratory informatics needs. Through world-class people, process, and technology, Astrix works with clients to fundamentally improve business, scientific, and medical outcomes and the quality of life everywhere. Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of fully integrated services designed to deliver value to clients across their organizations.