have confidence at every turn

Clinical trials are fraught with missteps and inaccuracies that can create costly delays. Remove uncertainty and risk from your clinical research to move ahead quickly — with confidence.

ENHANCE TRIAL OVERSIGHT

Run more efficient trials by unlocking hidden insights in your data

ENABLE SITE OPTIMIZATION

Generate better data by optimizing site selection and performance

INCREASE PATIENT ENGAGEMENT

Equip patients with the right tools to take control of their health

ENSURE SAFETY AND MEASURE EFFICACY

Drive high-quality eCOA, cardiac safety, respiratory and imaging data

ENHANCE TRIAL OVERSIGHT

RISK MANAGEMENT

Predict potential risks before they happen and identify areas for proactive mitigation with predictive analytics and automated alerts.

REAL-TIME INSIGHTS

Protect your development pipeline, clinical trials and ─ most importantly, your patients ─ with real-time visibility across all trial stakeholders.

ACTIONABLE INTELLIGENCE

Control your trial with actionable intelligence across studies, sites and patients by integrating all your clinical and operational data.

REPORTING SOLUTIONS

Get better visibility across all your ERT endpoint solutions via an array of reporting solutions and intuitive dashboards.

ENABLE SITE OPTIMIZATION

MITIGATE VARIABILITY

Mitigate inter-rater variability and reduce bias while improving patient compliance and engagement with on-device rater training.

CONSISTENT DATA

Improve the consistency and reliability of patient data with training on eCOA devices and software, patient care and protocol adherence.

BETTER PERFORMANCE

Minimize risks by ensuring the right sites are chosen and adequately prepared to support your trial.

COMPREHENSIVE TRAINING

Optimize performance and improve data quality with a blended approach to comprehensive site education and adaptable training.

INCREASE PATIENT ENGAGEMENT

Empower patients

Improve the patient experience wherever they are in their health journey and provide them with the right information at the right time.

Digital support programs

Deliver value and improve outcomes through fully-compliant support programs with personalized content and tailored interventions.

BYOD approach

Simplify post-approval data collection and reduce patient burden through engaging data capture programs that use patients’ own devices.

High-quality RWD

Have confidence in the quality of your patient-generated real-world data (RWD) and drive better-informed decisions.

ENSURE SAFETY & MEASURE EFFICACY

eCOA

Accelerate your research with technology that doesn’t get in the way using ERT eCOA.

RESPIRATORY

Demand data quality and breathe easy with ERT Respiratory.

CARDIAC SAFETY

Monitor every heartbeat with precision and ensure patient safety with ERT Cardiac Safety.

IMAGING

Minimize risks through high-quality data with ERT Imaging solutions.

moving ahead requires a sure path forward

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

a better way to manage your trials

Meet clinical development goals and achieve higher quality data, reduced costs, and shortened study timelines with support from ERT.

MINIMIZE RISK AND UNCERTAINTY

We deliver the flexibility and adaptability you need to overcome challenges 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.
25 ready-to-launch analytics tools
We protect  your trial before there’s ever an issue, ensuring its success through near real-time access to study, program and enterprise-level performance.

NEWS & EVENTS

LATEST NEWS

Paper vs Electronic Clinical Outcome Assessments

Join ERT and Helen Lundblad, PRO Manager from AstraZeneca, to explore paper vs. electronic collection. Electronic collection of clinical trial data has been recommended by the FDA since 2009 . While error-prone paper diaries introduce unnecessary risks into your study, using electronic Clinical Outcome Assessments (eCOA) has been shown to better engage patients, improve data quality and accelerate trials.

Accelerating Development

Here we review how a Risk-Based Quality Management (RBQM) approach to trial oversight can overcome many of the challenges facing clinical trial sponsors today ─ delivering the highest quality data, study performance improvements, and significant cost savings throughout their clinical trials.


3 Strategies to Capture ~ 100% Acceptable Respiratory Data in Clinical Trials

Collecting ATS/ERS-acceptable data is a fundamental goal for any pharmaceutical company involved in respiratory clinical trials. Here we present the three strategies clinical trial sponsors can adopt to ensure their data meets regulatory standards and helps them achieve their clinical objectives.