Smarter Clinical Supply. Delivered with Precision.
Datacapt Trial Supply Management brings real-time visibility and control to clinical supply logistics. Fully integrated with randomization and EDC workflows, it automates the entire supply chain, from kit assignment to site inventory, reducing risk, cost, and delays.
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Say goodbye to spreadsheets and disconnected systems.
End-to-End Supply Management & Logistics
Real-time visibility across sites, countries, and depots
Automated alerts for low inventory, resupply triggers, and expiry management
Full traceability from packaging to patient administration
Blinded & Unblinded Supply Support
Integrated with Randomization and eCRF
Automatically links supply assignment to randomization logic
Trigger kit assignment upon patient eligibility or visit completion
Configurable access control by site, depot, or sponsor role
Integrates with IWRS, depots, or CRO supply systems via API
Ready to Streamline Your Clinical Supply Chain?
Book a demo to see how Datacapt simplifies supply management with real-time control, seamless integration, and built-in compliance, designed for the demands of modern trials.
Trial supply management (TSM) refers to the planning, tracking, and delivery of investigational products to clinical sites and patients. It ensures that the right supplies reach the right place at the right time.
Yes. Datacapt offers an integrated RTSM module that combines real-time subject randomization with dynamic supply tracking and automated kit assignment—removing the need for third-party tools.
Yes. We support fully blinded, open-label, and mixed studies with masking controls and secure role separation.
Absolutely. Datacapt Medical Coding is fully 21 CFR Part 11 compliant, with electronic signatures, audit trails, and validation documentation available on request.
Absolutely. Datacapt provides real-time visibility of kit status at site and depot level, including stock levels, expiry dates, shipments, and returns.
Investigators can perform one-click emergency unblinding based on pre-approved permissions. Every unblinding action is logged with timestamp, user role, and justification to ensure audit-readiness.
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