Patient Data Reporting Solutions
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Phlexglobal Experts Fill The Gaps In eTMF Management
12/16/2022
Enable busy study teams to assess, prevent, and manage risk across the entire TMF spectrum – improving inspection-readiness with less effort.
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Bridging The Gap Between Research & Healthcare
10/1/2024
This platform offers precision source data capture, including secure EHR data retrieval to auto-populate trial eCRFs, a seamless user experience with single sign-on, and real-time data visualization.
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Aligning Site And Patient Needs For Clinical Trial Success
4/17/2025
Redefine clinical trial execution by aligning site and patient needs through a unified, intelligent platform.
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How To Achieve Timely Migration Of Your TMF
9/18/2023
This precise, proven methodology delivers a high-quality migration of your Trial Master File to the destination system, typically just 4-6 weeks after receiving all documents from the source system.
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Assess And Optimize Ratings Reliability
8/30/2023
See how this centralized solution for clinical ratings enhances the precision and dependability of data obtained from assessments based on clinician-reported outcomes (ClinROs), thus achieving elevated data quality.
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Industry-Leading Tech And First-To-Market Innovations Optimizes eTMF
3/14/2023
While an eTMF can be custom-configured upfront to meet the specific demands of a study, learn how IQVIA’s eTMF delivers the most advanced and sophisticated features and functionality available today.
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Technology Solutions And Services Tailored For Emerging Biopharma
1/16/2024
Explore how this collection of solutions and services is transforming clinical trials and empowering emerging biopharma organizations to revolutionize medicine.
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Adding eCOA To RTSM: Simplifying Workflow For Sites
12/9/2024
Simplify trials with Signant’s integrated SmartSignals eCOA and RTSM. Eliminate duplication, reduce reconciliation, and streamline operations for faster, error-free studies.
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High-Quality eCOA Implemented Rapidly
1/16/2024
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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Streamline Clinical Research With TrialMaster
1/27/2023
Organizations conducting clinical research can streamline the collection, processing, and submission of clinical trial data to regulatory authorities to expedite the development and approval to market life-saving drugs and devices.