Suvoda IRT

Command and control for clinical trial logistics

Managing patient randomization, drug dispensing, and supply forecasting across decentralized and hybrid trial models demands precision, flexibility, and responsiveness. Suvoda Interactive Response Technology (IRT) is designed to deliver exactly that—so that the right drug gets to the right patient at the right time.

Configured for real-world complexity

Built as modular components, Suvoda IRT offers extensive configurability for evolving study needs—from cohort and dose management to adaptive visit schedules and drug accountability. Study teams or project staff can implement mid-study changes directly, reducing reliance on change orders and supporting faster trial adaptations.

Scalable across patient and drug workflows

• Patient logistics: Supports adaptive replacement, cross-over designs, dose calculations, subject rollovers, and open-label extensions.
• Drug logistics: Includes dispensing, accountability, temperature excursion monitoring, controlled substances, variable sourcing, depot control, direct-to-patient shipping, and supply forecasting.

Elegant UI and reporting to guide decisions

Suvoda IRT balances power with clarity. An easy-to-use interface reduces cognitive load for users at all levels. Pre-set and ad-hoc visual reporting gives study teams real-time visibility into KPIs, site activity, drug availability, and depot status.

Empowering trials with powerful AI support

The safe and secure AI assistant, Sofia, transforms complex workflows, such as resupply planning and depot monitoring, into intuitive conversations. Clients can access vital logistics and trial data through a chat interface, streamlining what once required multiple screens into fluid interactions.

Key benefits at a glance:

• Centrally manage patient randomization and drug logistics with purpose-built precision
• A flexible solution that allows teams to implement some mid-study changes quickly through the user interface
• Harness AI-powered efficiency via Sofia’s chat interface
• Enable consistent trial oversight with real-time reporting and analytics