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  • 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 adverse [...]

  • Promotional graphic highlighting Fastrial AI+ for clinical trial execution, illustrating integrated eClinical software features such as EDC, ePRO, Safety & MedDRA, imaging, and LMS with human expertise oversight.
    AI/ML▪18th June 2026▪3.2 min▪

    Fastrial AI+: ICH E6 R3-compliant AI for trials

    Fastrial AI+ is the AI operating layer embedded across Medigen Suite, built for compliance with ICH E6 R3 and [...]

  • 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 [...]

  • 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 [...]

  • 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 integrated endpoint adjudication platform for DSMB committee reviews, featuring 21 CFR Part 11 compliant audit trails, SLA performance tracking, and live data capture integration.
    CTMS▪18th June 2026▪4.4 min▪

    The missing layer in clinical trials: real-time, approval-ready endpoints adjudication

    Clinical adjudication is where trials are decided Clinical adjudication is often described as a validation step. In reality, [...]

  • 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 [...]

  • eCOA vs ePRO: Getting Clinical Outcomes Right from Day One
    ePRO/eCOA▪18th June 2026▪3.8 min▪

    eCOA vs ePRO: what’s the difference?

    In modern clinical trials, the way you capture outcomes is no longer a technical detail—it is a strategic decision [...]