SUCCESS STORIES
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GxP Inventory Delivers Real-Time Visibility, Operational Efficiency
11/17/2025
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
11/17/2025
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
9/23/2025
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
7/15/2025
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
7/16/2024
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
6/17/2024
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
4/18/2024
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
4/17/2024
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
1/17/2024
Explore how these integrated solutions helped an emerging biopharma to implement a plan for study build and migration with minimal disruption to sites.
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eSource For A COVID Treatment Trial
1/17/2024
Unearth how this emerging biopharmaceutical company was able to overcome challenges to successfully facilitate a Phase 2 trial for a COVID-19 treatment in critically ill patients.