
Signant Health is the evidence generation company. We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies across traditional, virtual, and hybrid trial models. For more than 25 years, over 600 sponsors and CROs of all sizes – including all Top 20 pharma – have trusted Signant solutions for remote and site-based eCOA, EDC, eConsent, RTSM, supply chain management, and data quality analytics.
FEATURED CONTENT
An EDC Option You Didn’t Know You Had!
Signant Health offers the most comprehensive eClinical suite in life sciences, now featuring a recently acquired EDC/DDC solution proven in more than 3,000 clinical trials over 25+ years. Sponsors and CROs are switching to Signant Health's EDC for its ease of use, efficiency, flexibility, and superior support. Plus, study teams can choose a full-service or self-service model to accommodate the needs of any trial or program.
CLINICAL TRIAL OPTIMIZATION
Signant’s comprehensive, end-to-end clinical trial optimization solutions are fully supported by more than fifty full-time clinicians, scientists, medical practitioners, and key opinion leaders experienced in all therapeutic areas. In addition to reliable, proven solutions and scientific expertise, sponsors and CROs leverage Signant’s global scale and trial delivery expertise. Our approach to trial optimization is to ensure the best practices and best solutions are in place to help your programs succeed. Explore these resources to learn more about how this approach ensures trials generate reliable, accurate, submission-ready data.
RESOURCES & PERSPECTIVES
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Assessment Revolutionizes CNS Trial Outcomes: CDR Attention Battery
Discover how this validated 7-minute cognitive assessment transforms CNS trials through precise patient stratification, objective attention measurements, and enhanced signal detection.
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Beyond Diversity: Cultural Competence And Humility In Clinical Trials
Learn how cultural competence and humility transform clinical trials beyond diverse recruitment. Learn practical applications that enhance trust, improve data quality, and create more inclusive, effective research worldwide.
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A Data-Driven Approach To Clinical Trial Site Selection
By incorporating data-driven site selection and verification, sponsors can optimize resource allocation, enhance protocol compliance, and improve overall trial integrity.
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Cultural Competence And Humility In Clinical Trials
Cultural diversity in clinical trials is critical for generating meaningful and equitable healthcare solutions. However, achieving inclusivity goes beyond recruitment.
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Choosing The Right eClinRO Solution For Reliable Trial Data
Electronic clinician-reported outcomes (eClinROs) enhance the quality and consistency of clinical trial data. Discover key factors to consider when selecting an eClinRO provider.
SUCCESS STORIES
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RTSM And Clinical Drug Dispensation
A pharma company used Signant Health's RTSM solution in a Phase 2 schizophrenia trial to ensure drug availability, maintain study balance, prevent duplicate allocations, and manage returns and destruction of unused drugs.
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Our Unified Platform Serves As eSource For COVID Treatment Trial
Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.
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Consolidating Clinical Supply Chain Operations With GxP Inventory
A Japan-based biotechnology company leveraged Signant SmartSignals® GxP Inventory, which improved visibility, reduced risks and costs, and optimized operations in this case study.
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RTSM: Randomization And Cohort Management, IP Inventory Management
Signant’s SmartSignals® RTSM solution helped an innovative biopharmaceutical company secure an FDA Orphan Drug designation for its cardiomyopathy drug.
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Unified Platform Supports Rapid Implementation Of Rescue Study
Explore how these integrated solutions helped an emerging biopharma to implement a plan for study build and migration with minimal disruption to sites.
CONTACT INFORMATION
Signant Health
785 Arbor Way
Blue Bell, PA 19422
UNITED STATES
Phone: 610.400.4141
EVIDENCE GENERATION
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Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.
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Utilized in over 3,000 clinical trials, learn about this comprehensive EDC solution that delivers high-quality data on time and addresses any study team's goals.
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Utilize this eCOA module within the Signant SmartSignals Unified Platform to take advantage of a flexible and modern application designed for convenient at-home completion.
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This EDC and DDC solution has supported over 3,000 clinical trials over 30 years. Experience the simplicity, flexibility, efficiency, and superior service you’ve been missing from your EDC.
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With a proven track record in thousands of trials and contributions to numerous novel drug approvals, Signant SmartSignals eCOA stands as the ultimate electronic data capture solution in the industry.
IP MANAGEMENT
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Discover how Signant SmartSignals RTSM ensures the right patients get the right medications at the right time.
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Embark on a journey to uncover six compelling reasons behind adopting this RTSM solution, which boasts a modern front-end interface, for your upcoming study.
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Managing clinical trial supplies is challenging. GxP Inventory streamlines the process, providing full visibility into inventory, genealogy, and quality release in one system.
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Empower direct-to-patient clinical supply distributions with Signant's RTSM solution.
APPLICATIONS & THERAPEUTIC AREAS
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Explore how this collection of solutions and services is transforming clinical trials and empowering emerging biopharma organizations to revolutionize medicine.
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Uncover how this unified platform is helping sponsors and CROs generate high-quality data, accelerate trials, and rapidly scale to Phase 2 and beyond.
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Delve into how Signant Health's SmartSignals solutions and services effectively bolster decentralized clinical trials (DCTs) and the seamless execution of remote trial activities.
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Learn how our expertise in eCOA, RTSM, and eConsent solutions can accelerate your drug development program from early phases to regulatory approval.
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Explore how Signent's offerings aid CNS research teams in enhancing the efficiency, effectiveness, and global impact of their studies, for the benefit of all participants involved.