Clinteract: Randomization and Trial Supply Management Solution
Clinteract is Sharp’s Interactive Response Technology (IRT) solution for full-service Randomization and Trial Supply Management (RTSM). Purpose-built to simplify and streamline complex clinical trial processes, Clinteract supports patient randomization, clinical supply management, site inventory oversight, and visit scheduling. Designed for flexibility, integration, and real-time control, it’s ideal for complex trial designs requiring high configurability, operational efficiency, and data integrity.
Clinventory: Clinical Inventory Management System
Clinventory is Sharp’s flexible, streamlined solution for clinical trial supply chain management – ideal for studies that don’t require full IRT functionality but need more than a spreadsheet. Designed for Early Access Programs and simpler trials, Clinventory offers intelligent automation, real-time visibility, and centralized control across multiple protocols. With end-user configurability and smart resupply planning, it helps optimize inventory, reduce waste, and simplify site operations.
Clinical Supply Manager Consultancy
Sharp’s Clinical Drug Supply Managers (DSMs) are experts in managing clinical trial supplies across all study phases and designs. Their deep expertise includes oversight of IRT systems, supply strategies, and blinding requirements. With their proactive approach and strategic insight, DSMs become an extension of your trial team – ensuring efficient supply operations, minimizing risk, and supporting the overall success of your clinical trial.
Clinteract vs. Clinventory
| Feature/Functionality | Clinteract | Clinventory |
| Type of Solution | Interactive Response Technology (IRT) / Randomization and Trial Supply Management (RTSM) | Clinical Inventory Management System |
| Primary Purpose | Manages patient randomization, drug supply management, and site inventory | Manages drug ordering and site inventory when full IRT functionality is not needed |
| Primary Use Case | Complex clinical trials requiring patient randomization, visit tracking, blinding management, and full supply oversight | Early Access Programs or simpler studies requiring inventory oversight without IRT functionality |
| Patient Tracking | Yes | Not supported |
| Randomization Capability | Full support for complex randomization schemes | Not supported |
| Visit Schedule Management | Yes | Not supported |
| Drug Supply Management | Yes | Yes |
| Drug Accountability | Yes | Yes |
| Returns & Destruction Tracking | Yes | Yes |
| System Flexibility | Highly configurable based on protocol and trial complexity | Flexible with both automated and ad hoc drug ordering |
| User Configuration | End-user powered with role-based permissions, aligns with complex trial workflows, and supports post–go-live configurable parameter settings—reducing the need for formal change controls | The system is end-user powered and supports post–go-live configurable parameter settings, reducing the need for formal change controls |
| Ideal Use Case | Clinical trials requiring subject randomization, visit management, and full supply chain visibility | Ideal for trials or Early Access Programs that require drug inventory management without patient-level tracking, and for studies that don’t need full IRT functionality but require more structure and visibility than spreadsheets can provide |
| Reporting & Visibility | Real-time insights across randomization, inventory, and dosing schedules | Real-time inventory tracking and reporting across sites and depots |
