Change With Your Protocol
Update recruitment controls, inventory settings, and operational parameters, access reports, and make authorized data corrections yourself, so mid-study changes happen fast.
A cloud-native IRT platform that connects randomization, participant management, clinical supplies, and reporting. When your protocol changes mid-study, your team makes many updates directly, without waiting on a vendor change request.
Self-service mid-study changes • 24/7/365 support • 158+ countries supported
Clinical trial teams need to manage participants, sites, inventory, supplies, and study operations without losing visibility or agility. ClinPhone Pro brings these critical workflows together in a single connected platform, giving a real-time view across study operations, participant management, randomization, inventory, logistics, and reporting.
Update recruitment controls, inventory settings, and operational parameters, access reports, and make authorized data corrections yourself, so mid-study changes happen fast.
Make operational updates, access reports, manage recruitment controls, and perform authorized data corrections through self-service tools.
Stay ahead of demand with automated resupply planning and one-click Forecast Order.
Accelerate study delivery with configurable templates, reusable libraries, and rapid system demonstrations.
Connect seamlessly with EDC, eCOA, CTMS, inventory systems, and other clinical technologies.
Configurable workflows tailored to study phase, therapeutic area, and protocol requirements.
Cohort management, blocked and dynamic randomization, participant replacement, recruitment controls, and emergency unblinding.
Screening, enrollment, visit schedules, visit modifications, withdrawals, participant data updates, and direct-to-participant workflows.
Inventory optimization across depots and sites with automated resupply, lot and expiry management, and reconciliation.
Depot-to-depot, depot-to-site, and site-to-site shipments while forecasting future demand and maintaining continuity.
Dashboards, audit trails, data change reports, participant history, inventory tracking, and operational analytics.
Forecast future shipment requirements and generate replenishment orders with a single click, helping sites and depots maintain supply readiness.
Monitor participant actions, inventory movements, shipments, data changes, and user activities through comprehensive audit history and reporting.
Make immediate study updates and operational adjustments yourself, so mid-study changes do not queue behind a change request.
Monitor enrollment, inventory levels, site activity, participant visits, and study performance from a unified platform.
Control recruitment, enrollment, cohorts, and study oversight.
Forecast demand, optimize inventory, and manage resupply.
Complete study tasks faster with guided workflows and intuitive screens.
Access reports, trace changes, and maintain auditability.
Integrate easily with scalable cloud-native architecture.
Engineered for scalability, resilience, disaster recovery, and global deployment.
Independent services enable faster deployment, easier maintenance, and simplified integration.
Pre-validated template libraries support rapid study deployment while maintaining consistency and quality.
Integrates with EDC, eCOA, CTMS, inventory management systems, depot systems, and broader clinical ecosystems.
ClinPhone Pro is supported by dedicated RTSM specialists embedded throughout the study lifecycle.
ClinPhone Pro is designed to support the regulatory and quality requirements of modern clinical trials.
Dedicated quality and compliance teams support sponsors, CROs, and sites through audits and inspections, with rapid document access and structured oversight.
Bring randomization, participant management, clinical supply operations, inventory control, logistics, and reporting together in a single cloud-native platform built to support global clinical trials.