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Outcomes Analytics

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23 - Outcomes Analytics
Add an additional layer of quality control to clinical data

Identify threats to endpoint quality

Proprietary algorithms and intuitive visualizations help study teams verify raters and sites are generating valid, verifiable, and accurate data.

Verify protocol adherence

Examine study data at multiple levels to ensure consistent performance across raters, sites, regions, or studies.

Prevent data invalidation

Proactively intervene to correct issues that, if left unchecked, could propagate throughout your study data.

How does outcome analytics work?

Signant SmartSignals Outcomes Analytics examines study data at all relevant levels (rater, site, country, region, and study) to identify clinically relevant quality concerns and presents findings in graphic visualizations, making interpretation and analysis simple.  

Your team will be able to monitor the collected data quality throughout the course of the trial using a variety of views and outputs to extract key insights, such as verifying that sites are adhering to protocol requirements. 

Why choose Signant SmartSignals? 

Signant Health combines clinical and data science to help you maximize your study’s potential and monitor performance with greater clarity. We provide not just eCOA technology, but the scientific advisory and business intelligence you need to deliver primary and secondary endpoints with confidence in data quality and accuracy. Explore our full Signant SmartSignals suite of end-to-end solutions to see why sponsors and CROs rely on Signant Health for optimized evidence generation.  

FAQs

Can clinical outcome analytics be performed for any indication?

Outcome Analytics provides centralized statistical review of eCOA data for any therapeutic area or indication. Signant Health will tailor the clinical data analyses based on the data collected.

How is Outcome Analytics different from the standard dashboard reporting of eCOA data?

Outcome Analytics goes beyond standard eCOA reporting by deploying statistical analyses to identify data manipulation, fraud, carelessness, or other indicators of poor clinical data quality.

What is risk based monitoring (RBM) in clinical trials?

Risk-based monitoring is the process of ensuring the quality of clinical trials by identifying, assessing, monitoring and mitigating the risks that could affect the quality or safety of a study.

Can you provide scientific consulting to support our eCOA approach?

Signant proudly provides expert consulting with our solutions, like eCOA. We believe that combining our advanced technology with scientific and clinical expertise properly sets studies up for success. Our focus on protecting data quality along with our credibility among authors and license holders helps us successfully navigate electronic implementations. With a deep understanding of regulatory needs, our team can help steer clients throughout their clinical trials.

Can Signant implement computerized adaptive tests (CATs)?

Yes. Signant SmartSignals eCOA includes the ability to implement the PROMIS CAT seamlessly alongside conventional PROMS. Choose from more than 20 domains including anxiety, depression, fatigue, sleep disturbance, pain interference, physical function, and social function. For more information, read our PROMIS CAT brochure and white paper.

Want to learn more?

Ensure data integrity throughout your clinical trials by leveraging Signant's proprietary algorithms and intuitive visualizations to identify threats, verify protocol adherence, and prevent data invalidation effortlessly.

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