CISYS LifeSciences

Accelerate clinical trial document exchange with a secure, centralized platform. Redaction, version control, and compliance built in — no more email chains or missing files.

Seamlessly manage document workflows and integrate with study systems like EDC, CTMS, and safety platforms. All in one compliant portal.

If your study teams still manage critical documents through emails and attachments, there’s a better way. WebFXP centralizes communication and reduces delays.

Evaluate inclusion/exclusion criteria across all sites using a streamlined, compliance-ready platform built for precision and scale. Whether your priority is speed or sophistication, WebPatient adapts to your trial’s needs. Designed to streamline eligibility workflows without compromising compliance, WebPatient offers two purpose-built options, each delivering clarity, consistency, and control.

Streamline clinical trial readiness and guarantee GxP compliance across every study site. Discover the LMS built specifically for the rigorous regulatory demands of life sciences, pharma, and biotech operations. Automate training logs, simplify protocol updates, and stay permanently audit-ready.

WebFXP was designed for real users. This includes site coordinators, investigators, research nurses, project managers, and all clinical professionals who keep studies moving each day. It is clear and intuitive and feels familiar from the first login.