Your Research is now part of the Almac Group. Read more here about this strategic acquisition. 

Best in-class technology; unparalleled service

eCOA excellence

Your Research’s electronic Clinical Outcome solution transforms how clinical trials collect and manage patient-reported outcomes.

With an emphasis on real-time data capture, ease of use, and compliance, our eCOA system enables participants to provide accurate data directly from their devices.

This intuitive solution enhances data quality and engagement, delivering timely insights to sponsors and CROs while reducing administrative burdens and ensuring protocol adherence.

Real-Time Data Collection

Immediate data capture from patients, caregivers, and clinicians, improving data accuracy and study responsiveness.

Enhanced Participant Engagement

Simple, intuitive interface designed to boost compliance and participation, making it easy for patients to complete assessments.

Global Compliance Standards

Fully compliant with regulatory requirements, including 21 CFR Part 11, GDPR, and GCP, ensuring secure and reliable data handling.

Human Connection

Designed to emphasise the crucial role of human interaction in driving engagement and improving trial outcomes.​

eCOA Electronic Data Capture (EDC) 21 CFR Part 11 Compliance Patient Monitoring eConsent HIPAA Compliance Document Management Audit Trail Workflow Management Cloud-Based CTMS Remote Patient Engagement

Key features

Seamless, secure, and engaging data collection

Leveraging both retrospective and prospective insights, our intelligent workflow guidance supports efficient and accurate trial management.

By providing an exceptional experience, timely notifications, and enhanced usability for participants, we effectively mitigate both study protocol adherence and patient retention risks.

Validation Data Collection

Pre-validated or tailored questionnaires including real-time data validation checks and reminders to ensure completeness and accuracy of the clinical trial data.

Smart Participant Retention

Your Research employs smart participant retention methods to keep participants engaged and committed throughout clinical trials. These include personalized communication, flexible scheduling, gamification, and real-time feedback, all seamlessly integrated into our platform. By enhancing the participant experience and reducing administrative burdens for sites, Your Research ensures higher retention rates and more reliable trial outcomes.

 

 

Multiple Formats

eCOA includes questionnaires, scales, and diaries that can be tailored to the study's requirements and are designed to be user-friendly for accurate self-reporting.

Modular Technology

Featuring a single user-personalized interface for study oversight, Your Research streamlines operations and ensures seamless integration with other systems through Single Sign-On (SSO) and API capabilities.

eClinical Suite Electronic Data Capture (EDC) 21 CFR Part 11 Compliance Patient Monitoring eConsent HIPAA Compliance Document Management Audit Trail Workflow Management Cloud-Based CTMS Remote Patient Engagement

Types of Assessments

Your Research facilitates efficient data management, organisation, and analysis, enabling study teams to proactively access and analyse patient-reported data more easily.

Our services

Streamline service delivery to minimize risks and expedite startup

Minimising startup and delay risks is the goal of our services. Whether you prefer a hybrid or full self-service model, we are ready to assist with our expertise and experience, ensuring peace of mind.

Validated Questionnaire Libary

Pre-validated questionnaires will save you time setting up your trial and data quality risks

Translation Services

Our network of translators will support with validated translation of questionnaires and communication information for participants.

IRB Submission Support

Together with our technology, local partners and pre-defined documentation, we support you to have oversight into your IRB approval process.

Device Provisioning

Your Research provides pre-configured devices to patients for consistent performance and controlled study environments based on a hybrid or full provisioning model.

Global Support and Training

We provide 24/7 assistance to address technical issues and user inquiries, as well as training for clinical staff to ensure they are proficient in using Your Research.

Compliance for Global Trials

Your Research complies with international standards and regulations, ensuring data security and privacy across all operational regions.

Modules at a glance

Elevate the whole Participant Journey

Serving as the essential foundation, our Unified Protocol facilitates the seamless integration of both modules and third-party systems along the Participant Journey. 

This foundational structure ensures comprehensive oversight and enables strategic foresight throughout the patient journey.

More information?

Contact us for more information how to use Your Research in your trial.