Clinical solutions reimagined - delivering value with GenAI

    From accelerating clinical study report generation by 30%–50% with over 90% accuracy to converting unstructured health records into structured data, Axtria’s GenAI solutions are creating true value for its customers.
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    Transform clinical study report generation with GenAI

    Axtria's innovative GenAI solution slashes clinical study report creation time by 30%-50% and reduces the manual effort and errors significantly to help bring the life-saving treatments to the patients faster.

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    Transform clinical study report authoring process with GenAI powered automation

    Harness the power of GenAI to accelerate clinical study report authoring process, enhance accuracy, and ensure regulatory compliance.

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    Overcome challenges in clinical data workflows through clinical information management

    Axtria’s core clinical information management capabilities encompass consulting & execution for clinical data platforms and implementation services.

    Our clinical experts and SMEs advise on enterprise architectures & solution roadmap; industry trends and maximizing ROI; metadata repository and master data management; change management and migration strategy; GxP compliance; data governance; data lineage and traceability; CDISC, SDTM, ADaM; RWD & EHR, HL7, FHIR:

    • Clinical data strategy design & implementation
    • Clinical data management, warehousing, & system integration
    • Governance, clinical standards & terminologies, quality
    • Study insights & operational reporting, dashboarding

     

    Clinical Solutions_ Innovating to transform clinical research, bolster trial success, and improve patient outcomes

    Enhance the value of trial insights with clinical data science

    Leverage Axtria’s deep domain and consulting expertise in data science to maximize the value of insights generated from clinical trials; find and tell the hidden story in the data supporting product value proposition.

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    ML-based trial performance, recruiting, and likelihood of success

    Machine Learning & Predictive AI to assess clinical protocols, site and patient fit for optimizing patient recruitment & trial performance.

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    AI enabled site & patient engagement

    AI-driven insights to enhance site identification, patient recruitment and retention, overall trial efficiency for accelerated clinical success.

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    Gen AI applications with study data

    Unlock the potential of Gen AI to automate clinical trial data curation, analysis, and reporting to drive efficiency and innovation in clinical study workflows.

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    ML framework and operations

    Accelerate clinical trials with ML and MLOps, ensuring efficient model deployment, continuous monitoring, and scalable AI-driven insights for data-driven decision-making.

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    Patient matching to clinical trials

    Enhance trial efficiency with AI-powered patient matching, identifying eligible participants faster while improving recruitment precision and trial outcomes.

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    ML-based clinical data monitoring

    Ensure data integrity and compliance with AI/ML-driven monitoring, enabling real-time insights and proactive issue detection in clinical trials.

    Axtria clinical innovation supports faster, better trials

    Clinical trial optimization

    • Expert designed and data informed clinical trial protocol
    • Testing trial inclusion/exclusion criteria against real-world data
    • Analysis/re-analysis of de-identified electronic health record data
    • Integration of social determinants of health data for trial diversity, equity, and inclusion

    Site selection

    • Identify relevant patient populations and where they are located
    • Link physician national provider identifier number to reach out to facilitate trial recruitment
    • Determine site feasibility based on operational performance, available patients, competing trials, and potential research fatigue

    30%–50% faster CSR authoring

    • Accelerate generation of first draft clinical study reports using GenAI
    • Input tables, listings, and figures and output narrative summaries of high-level results
    • Prompt engineer with iterative feedback from experts for scientific tone and preparation for regulatory submission
    • Substantially reduce NDA approval timelines

    Our work in late phase investigations supports a variety of study objectives and designs

    Support for clinical research strategy and operations

    • Trial design and optimization
    • Promotional regulatory strategy
    • Site selection and support
    • Clinical analytics and data science
    • Data management and analysis
    • Promotional regulatory support
    • Clinical study report authoring

    Post-launch prospective data collection

    • Multi-pronged approach with multiple data partners for comprehensive identification and collection of fit-for-purpose prospective data
    • Integration across data types, including consented trial data, linked tokenization to administrative claims, wearable devices, digital data, social determinants of health, etc.
    • Registry-like data capture system for longitudinal tracking

    Phase IV randomized controlled trial

    • Support limited areas of the investigation consistent with our business and areas of expertise
    • Manage the overall Phase IV program as coordinating PMO
    • Vendor selection and management (CRO, labs, IRT, data management)
    • Ownership of RWD/E or any additional pragmatic components

    Pragmatic trial investigations

    • Support the full scope of the investigation
    • Trial design, feasibility
    • Statistical analysis plan
    • Site contracting (through robust site network partnerships)
    • Trial initiation, conduct and closure
    • Data Pipeline, primary data collection
    • Operational dashboarding
    • Integration of RWD data/endpoints
    • Regulatory package preparation and submission support

    Simplify clinical trials through solutions and innovations that maximize return on investment

    Better designed trials for the right patients and endpoints

    Reduce errors through good data management and science

    Enhanced solutions Phase I-IV for continuity and ongoing support

    Innovations transforming clinical research to improve patient care

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    What are Axtria Clinical leaders thinking about?

    White Paper

    GenAI-Enabled Automation to Eliminate Clinical Trial Data Bottlenecks and Errors

    White Paper

    30%–50% Faster Clinical Study Reports with Generative Artificial Intelligence-Powered Automation

    White Paper

    Digital Twins: A Fit-for-Purpose Solution to Elevate Clinical Trial Power and Efficiency