Late Phase Trials

IP supply

IP Supply is an intelligent clinical supply management solution designed to simplify and control drug logistics in late-phase clinical trials. With real-time visibility into inventory, shipments, and site-level demand, it ensures uninterrupted trial supply, reduces wastage, and optimizes medicine shelf life across global sites and CROs.

Key Benefits

1

Reduced Wastage

Minimises overall drug wastage by aligning supply levels with actual trial demand and consumption patterns.

2

Shelf-Life Optimisation

Optimises medicine shelf life through controlled distribution and timely re-supply decisions.

3

Supply Continuity

Ensures uninterrupted availability of investigational product across all clinical trial sites.

4

Operational Efficiency

Simplifies supply operations by automating re-ordering, shipment management, and coordination tasks.

5

Improved Collaboration

Strengthens coordination between sponsors, CROs, and sites for faster, aligned supply decisions.

6

Inspection Readiness

Facilitates easy audits with complete, accurate, and traceable supply documentation.

Key Functionalities

Inventory Automation
Automates inventory re-ordering and stock management based on real-time consumption and predefined thresholds.
EDC Integration
Ensures compatibility with third-party EDC systems to align supply planning with enrolment and visit data.
Audit Traceability
Maintains complete, time-stamped audit trails to support inspections and regulatory reviews with ease.
Dashboard Analytics
Provides real-time dashboards and analytics to monitor inventory status, demand trends, and supply risks.
Shipment Control
Manages end-to-end shipment activities, including returns and cancellations, without operational complexity.
Site Collaboration
Enables seamless collaboration between trial sites and CROs through shared, real-time supply visibility.
Demand Planning
Supports proactive planning of medicine supply needs to prevent stock-outs and overstocking.
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reduction in overall drug wastage across clinical trials

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improvement in medicine shelf-life utilisation through proactive inventory and supply planning

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reduction in manual effort for supply management and site coordination activities

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traceability of drug supply records to support regulatory inspections and audits

Let's understand how you manage your Late Phase Studies?