MOVING AHEAD REQUIRES A SURE PATH FORWARD

Trials are inherently risky, and every detail matters. We spot risks before they become problems to help you avoid costly delays through an array of solutions that provide confidence at every turn.

ENHANCE TRIAL OVERSIGHT

Run more efficient trials by unlocking hidden insights
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enable site optimization

Generate high-quality data by optimizing site selection and performance
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increase patient engagement

Equip patients with the tools to take control of their health
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ensure safety and measure efficacy

By driving high-quality data
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THE ERT EXPERT PLATFORM

The ERT EXPERT® platform is the underlying proprietary technology that powers all ERT solutions. Improve trial visibility and performance and reduce time-to-market with confidence, agility and acceleration.

MINIMIZe RISK AND UNCERTAINTY

We enable the flexibility and adaptability you need to accelerate through hurdles for faster speed to market. Here’s how:

 

235k investigative sites supported

Every trial runs into unexpected challenges. With more than 13,000 trials under our belt, we’ve seen most of them before and have the expertise to put your trial back on course.

 

13K+
Trials supported
25 ready-to-launch analytics tools

We’ll protect the success of your trial before there’s ever an issue, with near real-time access to study, program and enterprise-level performance.

 

3M+
global patients supported

NEWS & EVENTS 

LATEST NEWS

Four Steps to Implementing Risk-based Quality Management

Learn how a Risk-based Quality Management (RBQM) approach to trial management ─ including technology that integrates data from multiple sources for real-time decision making ─ helps sponsors and CROs mitigate clinical trial risks before they become costly problems.

Putting Patients First – Building Adaptive Digital Health Programs

This article reviews how the ERT/Foundry3 collaboration is delivering rich, adaptive digital health programs ─ based on substantiated patient needs ─ to help patients better manage their conditions and ultimately improve health outcomes.


Why Early Phase Cardiac Safety Assessment Makes Good Business Sense

Learn how determining the cardiac safety profile of your compound by assessing QT during routine Phase I studies enables you to make go/no-go decisions sooner, better prioritize your drug development pipeline, and appropriately resource or refocus programs exhibiting potential cardiac safety issues.