• Banner graphic demonstrating how Medigen Suite integrates CDISC standards into eCRFs from day one, converting clinical data standards into SDTM and ADaM submission-ready datasets for accelerated regulatory filings.
    CTMS, EDC▪24th June 2026▪6.5 min▪

    CDISC compliance built for faster trial submissions

    Many data managers encounter CDISC issues later than ideal in the study timeline. A field gets mapped inconsistently across [...]

  • Banner graphic for Catchtrial Safety software highlighting auditable endpoint adjudication, DSMB and CEC workflows, automated event allocation, and real-time concordance analytics for clinical research sponsors.
    EDC▪19th June 2026▪6.1 min▪

    Smarter Endpoint Adjudication for Clinical Event Committees and Sponsors

    When a serious cardiac event occurs at one site and a similar event occurs at another, sponsors need to [...]

  • Header graphic featuring Mastertrial LMS+ software on a laptop screen, highlighting study-specific eLearning, real-time dashboards, and certified training records designed to streamline protocol training and site readiness prior to site activation.
    eLearning▪18th June 2026▪5.8 min▪

    Confident Protocol Training for High Performing Study Sites

    Clinical trials rarely fall behind because of a single major issue. More often, delays begin with inconsistent training, incomplete [...]

  • Infographic displaying an all-in-one CTMS clinical trial management system dashboard showing live data analytics for active studies, open issues, CRA monitoring visits, and site readiness metrics.
    CTMS▪18th June 2026▪3.9 min▪

    Clinical Trial Management System: Oversight to Insight

    How Maptrial CTMS+ software supports monitoring, training, and performance oversight in modern clinical studies As clinical trials increase [...]

  • Infographic displaying an EDC-integrated clinical trial imaging solution for imaging CRO teams and core lab reviewers, featuring real-time DICOM viewer capabilities, AI anonymization, and audit-ready data security.
    Medical Imaging▪18th June 2026▪2.9 min▪

    Clinical Trial Imaging: DICOM & Core Lab in Your EDC

    Integrated DICOM Imaging, Core Lab Workflow, and AI-Powered Compliance When imaging works seamlessly, everything moves faster In [...]

  • Visual guide detailing Catchtrial EDC+ CDISC data journey, incorporating CDASH, SDTM, ADaM, and Define-XML alongside MedDRA coding and WHO Drug Dictionary dictionaries for safety data standardization.
    EDC▪18th June 2026▪7.1 min▪

    CDISC Standards Explained: SDTM, ADaM, CDASH

    What Are CDISC Standards? CDISC standards are a globally recognized set of data standards developed by the Clinical [...]

  • Banner diagram explaining automated MedDRA coding for adverse events, highlighting time savings, consistency, and WHO Drug Dictionary integration for audit-ready safety data.
    EDC▪18th June 2026▪8 min▪

    MedDRA Coding: How Auto-Coding Saves Hours per Study

    What Is MedDRA Coding — and Why Does It Matter? MedDRA coding is the process of translating free-text [...]

  • Educational graphic detailing the transition from ICH E6 R2 to ICH E6 R3 GCP compliance standards in Catchtrial EDC+, showcasing risk-based oversight, data integrity safeguards, and global regulatory readiness for FDA, EMA, and PMDA.
    EDC▪18th June 2026▪7.2 min▪

    ICH E6(R3): How Your EDC Should Adapt to New GCP Rules

    The ICH E6(R3) guideline, finalized in January 2025, represents the most significant rewrite of Good Clinical Practice standards in [...]

  • Header graphic showing Mastertrial LMS+ on a laptop with study training progress bars, highlighting a 21 CFR Part 11 LMS and validated LMS built as a dedicated training management system for clinical trials.
    eLearning▪18th June 2026▪6.7 min▪

    Training Management System: Why Trials Need a Dedicated Validated LMS

    Summary: As clinical trials become increasingly complex, training management can no longer be treated as a purely administrative function. [...]