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SCIENTIFIC EXPERTISE

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Backed by our team of over 50 full-time clinicians, scientists, and medical practitioners, along with comprehensive scientific advisory boards comprising key medical opinion leaders across all disease areas

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Comprehension is key

At Signant Health, successful eCOA isn’t just about our leading technology.  For successful trials, we combine our technology with robust clinical, scientific, and regulatory expertise to guide your study from design to regulatory submission.

With more than 50 full-time clinicians, scientists and medical practitioners, and comprehensive scientific advisory boards of key medical opinion leaders across all disease areas, we provide early study design consulting and COA selection expertise, develop optimal solutions with best practice implementation, and apply endpoint quality monitoring to drive highest quality clinical outcomes data you can rely on.

Science-Led Solutions and Consulting

Sponsors and CROs rely on Signant scientists to help their programs succeed.  Our science and clinical team provide expertise from study design to data interpretation, in areas including:

  • Study design & measurement strategy consulting
  • eCOA instrument design & adaptation
  • eCOA migration & implementation best practices
  • Scale and license management
  • eCOA modality consulting
  • PRO dossier support
  • Rater training & qualification
  • Central rating, central review, & central scoring
  • Patient eligibility & diagnostic review
  • Endpoint quality monitoring and data analytics
  • Placebo response mitigation
  • Evidence-based site selection

Key Services

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Study Design Consulting

Optimize your protocol design, ensure the best clinical outcome assessment measurement strategy, and implement successful approaches to optimize data quality.

 

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Scale and License Management

De-risk your study and reduce study team workload leveraging our scale and license experts to ensure the correct versions of measures are identified, the right licenses executed, and translations secured.

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Endpoint Quality Monitoring & Data Analytics

Drive endpoint accuracy and reliability through data quality analytics. Leverage our expert data scientists and proprietary tools to drive highest quality data from study start to close.

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Experts in All Therapeutic Areas

Our in-house clinical scientists and medical experts work across all disease indications and therapeutic areas to advance clinical development. With experience covering thousands of trials in 20+ therapeutic areas, you can count on us.

Therapeutic Area Expertise
Scientific Advisory Boards

Our Scientific Advisory Boards (SABs) play a pivotal role in shaping Signant's visionary approach to the clinical trials landscape, contributing to our forward-looking strategy, and providing important key opinion leader input in early protocol consulting and trial oversight.

Meet the SAB Members
Clinical Viewpoints

Our scientific and medical experts are practitioners in their own fields with deep, practical understanding. They consult on study design and measurement strategy, and optimal operationalization of study protocols. Learn more about our expertise and how it can apply to your development programs through our clinical viewpoints video series.

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Inside eCOA

When you use SmartSignals eCOA, you get not only our leading, innovative technology, but also access to our team of in-house digital health sciences experts who help study teams navigate common trial complexities. Explore some of our expertise areas thorough our Inside eCOA video series.

Watch the Series

Want to learn more?

Partner with us to ensure your clinical trials are scientifically sound, regulatory compliant, and efficiently managed

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