YPrime Patient Engagement is a cloud-based solution designed to support communication, adherence, and retention of participants in clinical trials. It provides digital tools that enable reminders, notifications, and structured interactions between study teams and participants. The system operates within regulated research environments and integrates with other clinical technologies to centralize participant-related activities and improve study continuity.

YPrime IRT is a cloud-based interactive response technology solution designed to manage subject randomization and clinical trial supply logistics. It supports allocation of participants to treatment arms, drug inventory tracking, and distribution workflows across study sites. The system operates within regulated clinical research environments and integrates with other clinical trial technologies to provide centralized operational control.

YPrime eCOA is a cloud-based electronic clinical outcome assessment solution designed to capture patient, clinician, and observer-reported data in clinical trials. It replaces paper-based instruments with digital questionnaires and diaries delivered via provisioned devices or bring-your-own-device models. The system supports regulated study environments with data validation, multilingual configuration, and integration into broader clinical trial workflows.

YPrime eConsent is a cloud-based electronic informed consent solution designed to digitize and manage participant consent processes in clinical trials. It replaces paper-based consent forms with interactive, multimedia-enabled workflows that support comprehension, documentation, and regulatory compliance. The system enables sponsors, sites, and CROs to track consent versions, capture electronic signatures, and maintain secure audit records within regulated research environments.

YPrime Technology Platform is a cloud-based eClinical system designed to support the execution of clinical trials. It provides electronic clinical outcome assessment (eCOA), electronic consent (eConsent), interactive response technology (IRT), and data management tools within an integrated environment. The platform enables sponsors and contract research organizations (CROs) to collect, manage, and monitor patient, site, and study data in regulated clinical research settings.