Signant is the evidence generation company that helps you digitally enable trials, no matter how or where you run them. We make the patient journey natural and intuitive, and the data journey direct and objective. Through the Signant SmartSignals® ecosystem, we deliver proof at the speed of life, simplifying and streamlining evidence generation while reducing reliance on paper-based processes. We offer vision at a time of change as well as reliability and dependability where it matters most. When the world is counting on you, count on Signant.
FEATURED CONTENT
An EDC Option You Didn’t Know You Had!
In the face of escalating costs and growing complexities in clinical development, success demands the right combination of resources, expertise, and speed. 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.
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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De-Risking Schizophrenia Trials: Strategies For Improving Signal Detection
Here, we summarize a recent webinar on the importance of integrating science-driven decision-making with proactive operational measures to safeguard both trial integrity and investment value in schizophrenia research.
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Modernizing Vaccine Trials By Leveraging eCOA And Harnessing Innovation
Explore how integrating eCOA, wearables, and AI-driven technologies can transform your vaccine trials for greater efficiency, patient engagement, and data quality.
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How CAR-T Cell Therapy And Digital Health Are Changing Cancer Care
As the next generation of cell-based therapies emerges, see why integrating digital health technologies will be essential for advancing efficacy, safety, and patient experience.
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Achieving End-To-End Clinical Supply Chain Visibility
Transform supply chain management by integrating technology solutions and real-time insights to link patient-level data with upstream manufacturing operations.
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How Cognitive Testing Transformed Narcolepsy Clinical Trials
From sleepiness scales to computerized cognitive testing, narcolepsy research now relies on tools like the CDR System to reveal the full impact of treatments on patients’ daily lives.
SUCCESS STORIES
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GxP Inventory Delivers Real-Time Visibility, Operational Efficiency
Modernize your clinical supply chain to streamline global trial operations, ensure regulatory compliance, and deliver investigational therapies to patients efficiently and reliably.
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Transforming Clinical Supply Planning From Spreadsheets To Smart Forecasting
Streamline your clinical supply forecasting and reduce risk by moving beyond manual spreadsheets to an integrated, real-time supply management solution.
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Streamlining Global Respiratory Trial Complexities With Robust Data Capture Strategy
Want to see how eCOA solutions can simplify patient-reported data capture and accelerate global trials? Explore implementation strategies, lessons learned, and measurable results.
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Analytics–Powered Approach To Patient Recruitment Strategy
In a Phase 3 psychiatry trial, a pharmaceutical company partnered with Signant to revolutionize patient recruitment through data-driven site selection using PureSignal Analytics.
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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.
CONTACT INFORMATION
Signant Health
785 Arbor Way
Blue Bell, PA 19422
UNITED STATES
Phone: 610.400.4141
CLINICAL DATA CAPTURE
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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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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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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.