With decades of experience, Premier delivers configurable, high-performance IRT and ePRO/eCOA solutions designed to simplify study management, enhance data integrity, and accelerate clinical trial timelines. Built on a robust, high-availability platform, our systems seamlessly support everything from patient randomization to decentralized trial workflows.

Interactive Response Technology: Comprehensive Trial Oversight From Site Setup to Last Patient Visit

Our Interactive Response Technology (IRT) platform is purpose-built to meet the dynamic needs of complex trials, with support for global logistics, real-time tracking, and integration with other clinical systems.

• Access & Permissions Management: Site, user, and system-level controls
• Visit & Cohort Management: Monitor patient progression from screening to follow-up
• Advanced Randomization: Central, stratified, dynamic, adaptive, biased coin
• Study Drug Management: Resupply automation, titration, and dose calculations
• Direct-to-Patient (DtP) Shipments: Enable decentralized and hybrid trial designs
• Drug Accountability & Expiry Management: Full chain-of-custody tracking
• Cold Chain Management: Controlled logistics for sensitive protocols
• Automated Reorders: Configurable thresholds and triggers
• Real-Time Reporting & Integrations: Live data feeds to CTMS, EDC, RBM, and more

ePRO/eCOA Platform: Reliable, Global Data Capture With Real-Time Oversight

Our ePRO/eCOA tools are designed to increase patient compliance, streamline data collection, and support global deployment—with seamless integration into your clinical ecosystem.

Key Features:

• Bring Your Own Device (BYOD), available as an App or on Browser​
• Configurable Reminders and Alerts
• Configurable Input Controls and front-end data capture​
• Real Time Compliance Monitoring​
• Real Time Reporting and Integration Capabilities​
• Multi-language compatible: Translated into over 50 Languages, including left to right languages, right to left languages, and character languages such as Hebrew, Arabic, and Mandarin​
• Support for assessment scoring
• Have received License Approvals for assessments across several therapeutic areas, including addiction medicine, analgesia, dermatology, general health, musculoskeletal disorders, neurology, oncology psychiatry/ psychology, and respiratory/ pulmonology.
• Caregiver Access capabilities​
• Access controlled Edit and Backfill capabilities ​
• Built to meet the highest global regulatory standards—21 CFR Part 11, GDPR, HIPAA, and GCP
• Built on Core High Availability IRT platform, allowing for seamless determination of enrollment eligibility

Why Choose Premier?

• Expertise You Can Trust: Our team brings decades of experience across hundreds of global trials. From strategy to execution, we deliver consistent quality and consultative support.
• Flexible by Design: Whether you need a rapid, configurable setup or a fully customized solution, our hybrid platform adapts to your protocol’s unique requirements.
• Faster Start Up:  Leverage rapid deployment options without compromising quality or compliance.
• Patient-Centric Innovation: Enable decentralized models with features like direct-to-patient shipments, multilingual ePROs, and caregiver functionality.
• Seamless Ecosystem Integration: Built to integrate with CTMS, RBM, EDC, eConsent, and more—our systems reduce data duplication and streamline study operations.
• User-First Interfaces: Designed for ease-of-use across all stakeholders, reducing training time and data entry errors.

Ready to Optimize Your Next Trial?

Contact Premier today to see how our IRT and ePRO/eCOA solutions can accelerate your timeline, reduce risk, and improve patient and site experience, either as a part of a full-service clinical trial solution or functional solution.