Electronic Data Capture (EDC) is the backbone of modern clinical data management. This collection covers eCRF design, data validation, medical coding, CDISC standards, and how a connected EDC supports cleaner data and faster database lock. Explore practical guidance for sponsors, CROs, and data managers running drug and device trials

  • 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 [...]