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Solutions

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

The 14th Annual Outsourcing in Clinical Trials (OCT) Southern California is being held in San Diego, CA this September 15-16, 2026. This conference brings together clinical operations professionals from pharma and biotech companies on the West Coast to discuss key challenges and how to make your clinical trial streamlined and efficient.

Mednet + CRScube will be exhibiting throughout the event, and we have a lot of new technology and capabilities to share.

Stop by our booth to get a closer look at what’s new, including:

  • AI-assisted EDC setup that turns CRF specifications into a configured study in days rather than weeks
  • Integration-free EHR-to-EDC that uses AI to identify and map source data directly into CRFs, reducing manual transcription at the site
  • AI-powered safety workflows for literature intake, signal detection, narrative drafting, and medical coding
  • Global safety reporting with direct regulatory gateway connections and expanded capabilities for medical device safety
  • Connected CTMS, eTMF, and RBQM to simplify oversight across the clinical trial lifecycle

Whether you’re looking to accelerate study startup, reduce site burden, improve data quality, or simplify safety operations, we’d be happy to show you what’s possible.

Stop by Booth #75 to explore what could make a difference for your upcoming studies.

To request a meeting with our team during the conference, contact us online or email Griffin Robertson at grobertson@mednetsolutions.com.