Objective, Clinician-Based Insights to Enhance Study Data
ClinRO
Clinician-Reported Outcomes (ClinRO) play a crucial role in capturing objective, professional insights into patient progress and treatment efficacy. At Your Research, our ClinRO module supports healthcare professionals in recording, managing, and analyzing clinician-reported data with ease, providing trials with accurate, reliable outcomes from trusted clinical perspectives.
ClinRO assessments provide a standardized, objective measure of participant health status and response to treatment, enhancing trial data with critical clinical observations.
With professional data entry from trained clinicians, ClinRO ensures that trial data is both robust and consistent, reducing variability and improving the accuracy of outcome measurements.
When combined with eCOA and ePRO data, ClinRO offers a full-spectrum view of treatment effects, blending clinician and patient perspectives for a more complete understanding of trial outcomes.
Key features
Core capabilities for accurate data capture
Your Research’s ClinRO module ensures that clinician-reported outcomes are captured accurately, securely, and in compliance with regulatory standards. By empowering healthcare professionals with the right tools and integrating with other outcome measures, we enable clinical trials to reach deeper insights and stronger, data-driven conclusions.
Equip clinicians with standardized tools and validated questionnaires that facilitate consistent, high-quality data collection. By ensuring assessments are performed uniformly, we enhance data reliability and support more accurate study conclusions.
Our ClinRO module integrates effortlessly with electronic Clinical Outcome Assessments (eCOA) and electronic Patient-Reported Outcomes (ePRO), bringing clinician, patient, and other stakeholder perspectives into a unified platform. This comprehensive data view supports holistic analyses of treatment impacts.
Clinicians can capture and upload assessments in real-time, allowing for timely monitoring and reporting of participant outcomes. The data is securely stored and readily accessible to authorized users, ensuring participant information is protected and readily available for analysis.
All ClinRO data is securely stored and organized to meet regulatory standards, ensuring compliance with ICH-GCP, FDA, EMA, and other global requirements. With trackable data trails and comprehensive audit logs, our system is always ready for regulatory review.
Built-in reminders help clinicians stay on track with assessment schedules, minimizing delays and keeping data collection aligned with protocol requirements.
Compliance for Global Trials
Your Research complies with international standards and regulations, ensuring data security and privacy across all operational regions.
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.
Pre-validated questionnaires will save you time setting up your trial and data quality risks
Our network of translators will support with validated translation of questionnaires and communication information for participants.
Together with our technology, local partners and pre-defined documentation, we support you to have oversight into your IRB approval process.
Your Research provides pre-configured devices to patients for consistent performance and controlled study environments based on a hybrid or full provisioning model.
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.
