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Guarantees safety, traceability, availability and integrity of data.

GCP and FDA 21 CFR Part 11 compliant, this proprietary software guarantees safety, traceability, availability and integrity of data from project design to database lock. It enables proactive study start-up management, direct electronic entry, information retrieval, and  CDISC standardized output to ensures tabulated, analyzable data throughout any project’s lifecycle.

A modular EDC platform with numerous advantages, it offers flexible solutions to manage clinical trial processes all in one place.

  • eCRF available in 5 languages
  • On-line Randomization
  • eSAE reporting
  • Drug handling and logistics
  • Data import from external sources (images, laboratory data, ePROs)
  • Protocol deviation (helps stay on track, on time on budget)
  • eLearning
  • Continuous support from our team


Clinical.net provides full integration, true customization continuous innovation and customer intimacy as a combination of features and benefits that give VALUE to clients.