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Mednet offers a unified clinical trial platform combining EDC, RTSM, CTMS, eConsent, ePRO, eTMF, safety, and intelligent automation — empowering sponsors and CROs to accelerate study startup, enhance data quality, and maintain continuity across all stages of clinical development.

Clinical EDC

October 14, 2026 at 11 am ET

Manual transcription of patient health records into EDC forms has always been a source of frustration for site users and a heavy workload for clinical research associates. While traditional EHR-to-EDC integrations exist to automate this transfer, they are frequently hindered by complex implementations, high costs, and site authorization requirements, leaving many clinical trial sites without a viable solution.

In this session co-hosted by CRScube and Mednet, we will introduce our new integration-free EHR-to-EDC feature. Attendees will view a detailed live demonstration showing how site staff capture data directly within cubeCDMS EDC without manual re-entry. The demo will showcase how this solution enables higher data quality while supporting remote source data verification, leading to a more efficient clinical data flow. Additionally, we will share how sponsors and CROs can deploy this capability universally across trial sites without technical integration hurdles.

Key takeaways

  • Eliminate errors at entry: Learn how integration-free technology replaces manual transcription and reduces data entry errors at the point of capture.
  • Reduce monitoring workload: Discover strategies to simplify source data verification (SDV) and decrease overall query management burdens.
  • Boost cross-functional efficiency: Explore how higher initial data quality elevates speed and productivity across monitoring and data management teams.

Register for the webinar >