ACCELERATE TIME-TO-MARKET BY UNLOCKING THE HIDDEN INSIGHTS IN YOUR DATA

ERT Trial Oversight is comprised of multiple applications that address critical areas of your clinical trials process: Trial Oversight Solution, Business Intelligence, and Real-Time Data Exchange.

ENHANCE TRIAL VISIBILITY
Achieve clarity across your clinical trials by seamlessly integrating all your critical trial data.

FOSTER UNRIVALED COLLABORATION
Drive collaboration among sponsor, CRO and vendor stakeholders.

QUICKLY MITIGATE RISK
Gain real-time access to trial performance, proactively mitigate risk and move ahead with confidence.

BEST PRACTICES FOR ICH E6 COMPLIANCE

Trial sponsors and CROs have struggled to comply with the ICH E6 Addendum since it took effect a few years ago. But besides the risks of non-compliance, you’re also missing out on the many benefits successful adoption can bring: proactive risk management, better trial performance, and on-time/on-budget studies. Have confidence in your approach to Addendum compliance with insights from our best practices guide.

TAKE A CLOSER LOOK

BROCHURE: ERT BUSINESS INTELLIGENCE SUITE

Get the reporting solution that best suits your needs and unlock hidden insights in your data.

BROCHURE: TRIAL OVERSIGHT SOLUTION

Proactively manage your clinical trial’s performance and risk in real-time. The ERT Trial Oversight solution helps put predictability, protection and control at your fingertips.

ADDITIONAL INSIGHTS

BEST PRACTICES GUIDE: SIX STEPS TO COMPLIANCE WITH ICH E6 ADDENDUM

Use this guide to better understand ICH E6 guidance on risk-based quality management and the implications for your trial, as well as our recommendations on how to get started on the path to compliance success.

ARTICLE: ACCELERATING DEVELOPMENT

The clinical trial industry is performing worse overall than a decade ago, and pharma has been slow to adopt new technologies that could reverse that trend. Learn how you can use technology and a risk-based managed approach to trial oversight to overcome challenges.