• Infographic detailing eCOA vs ePRO capabilities, comparing ePRO questionnaires and symptom diaries with eCOA clinician, observer, and performance outcomes managed within the Medigen Suite platform.
    ePRO/eCOA▪18th June 2026▪7.2 min▪

    eCOA, ePRO, or both? How to choose the right patient data strategy for your trial

    Summary: eCOA and ePRO are two of the most valuable tools available for capturing meaningful patient data in clinical [...]

  • 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 [...]

  • Explanatory banner showcasing how eMVR streamlines CRA monitoring and remote site monitoring through automated SDV tracking, real-time query visibility, protocol deviation management, and CFR Part 11 compliant audit trails.
    CTMS▪18th June 2026▪8.4 min▪

    eMVR: electronic monitoring visit reports explained

    Too Busy to Read the Full Article? Here's What You Need to Know An eMVR is an electronic [...]

  • 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 [...]

  • 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, [...]

  • 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 adverse [...]

  • Visual guide explaining why a unified eClinical platform and eClinical suite outperform siloed systems by connecting EDC, CTMS, eTMF, eMVR, site payments, ePRO, and eConsent in one eClinical software ecosystem.
    CTMS, EDC▪18th June 2026▪8.9 min▪

    eClinical software: the case for a unified platform

    Choosing the right eClinical software has become a genuine competitive advantage in clinical research. Sponsors and CROs now have [...]