Daniele Zago

Daniele Zago is COO and Chief Digital Officer at Meditrial, where he leads the R&D/IT behind Medigen Suite. With 20+ years of experience spanning eClinical software and quality management, he has led the design of FDA-compliant EDC and CTMS platforms and managed audits by Notified Bodies, Competent Authorities, and medical device manufacturers under ISO 9001, ISO 13485, and ISO 27001. He previously lectured on EU MDR 2017/745 at Università Roma Tre and writes Medigen Suite's eClinical series.

Daniele Zago is COO and Chief Digital Officer at Meditrial, where he leads the R&D/IT behind Medigen Suite. With 20+ years of experience spanning eClinical software and quality management, he has led the design of FDA-compliant EDC and CTMS platforms and managed audits by Notified Bodies, Competent Authorities, and medical device manufacturers under ISO 9001, ISO 13485, and ISO 27001. He previously lectured on EU MDR 2017/745 at Università Roma Tre and writes Medigen Suite's eClinical series.

Explore this author’s articles:

  • 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 [...]

  • 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 [...]

  • 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 [...]

  • 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 [...]

  • 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 [...]