Eliminate Trial Recruitment Delays
Over 80% of clinical trials experience enrollment delays due to inadequate feasibility. EFES transforms this process into a precise, digital science.
Integrated CDA Automation
Digital execution of Confidential Disclosure Agreements allows investigators to review protocol synopses instantly upon e-signing.
Pre-Prepared Questionnaires
Select from hundreds of therapeutic questions across oncology, neurology, infectious disease, or create custom protocol parameters in clicks.
Essential Document Portal
Site coordinators upload CVs, medical licenses, GCP certificates, and lab accreditations directly into the secure portal during evaluation.
Comparative Site Analytics
EFES aggregates site responses into ranked readiness scores based on competing trials, historical recruitment velocity, and facility equipment capabilities.
Export comprehensive feasibility reports for study steering committees and executive sponsors in seconds.
Experience EFES in Action
Request a tailored demonstration with sample protocols in your therapeutic specialty.