And that’s a wrap! Want to future-proof your clinical trials? Our eClinical platform supports all of the above workflow automation capabilities. Reach out to our team at contact@triall.io for more info. #blockchainforhealth #TRL #DeSci

⏩ Payments ⏩ Sites and participants often need to wait months before being compensated. Modern eClinical platforms tackle this issue by enabling automated payments based on completed study tasks & milestones, ensuring accurate & timely payment of key contributors.

⏩ Auto-validation ⏩ Study builders are increasingly using auto-validation simulators to validate their eCRFs against preprogrammed edit checks. This ensures data does not need to be entered by hand and often also auto-generates validation reports for future reference.

⏩ Cross-form edit checks ⏩ A unified eClinical platform brings various interoperability benefits. Notably, edit-checks between forms (e.g., eConsent form & eCRF) can trigger edit-checks and other conditional actions that help ensure accuracy, completeness, and consistency.

⏩ Direct data capture ⏩ Solutions such as eSource, ePRO, eConsent, and wearables allow data to directly flow into the EDC database. This eliminates the need to manually transcribe data from a paper chart or EHR, thereby promoting speed and lowering #SDV requirements.

⏩ Review workflows ⏩ Modern eClinical platforms enable review & sign-off workflows on a site, subject, visit, or data field-level. These workflows act as compliance stage-gates and promote efficiency by automatically notifying study monitors, data managers, and investigators.