Designed for zero product loss
SkyMind is the supply chain operating system that enables temperature-controlled shipments and proactively prevents product loss.
Create a resilient network
SkyMind combines operational data and simulation data to identify high-risk lanes that lead to product loss and then uses intelligent lane planning and temperature simulations to create scenarios that effectively reduce risks and improve your supply chain.
- Simulate lanes and shipment solutions
- Predictive simulation capabilities
- Extensive operational/ real-life data
- One platform integrating multiple logging solutions
- Centralized platform for shipment state and seal
- Intelligent alerts before incidents occur
- Make corrective actions and mitigate risk
- Identify and recommend alternative lanes
Any shipment. Any packaging. Any logger.
The SkyMind platform is fully interoperable with different container and packaging solutions and can be used across different modes of transportation.
End-to-end visibility for all
With SkyMind, all parties involved in the supply chain collaborate and communicate on the same integrated platform, from shipping to the release of the product.
All together on one platform
SkyMind is the supply chain operating system for managing operational risk. It helps you make sense of your entire dataset, and proactively recommends the actions to take to optimize the safety, security and sustainability of your shipment lanes.
Release products faster
Prevent theft and counterfeiting
Prevent product loss
Identify lane risks
Monitor shipment conditions in real time
Make corrective actions when needed
Generate reports and dashboards
Speed up validation time for new lanes
The SkyMind platform is certificated with the following set of quality standards:
ISO 27001 is the global standard for managing info security. It provides guidelines for establishing, implementing, maintaining, and enhancing security measures.
A quality management system that helps organizations be more efficient and improve customer satisfaction.
Guidelines for manufacturers and users of automated systems in the pharmaceutical industry.
21 CFR part 11
Rules which regulate the management and usage of electronic records in pharmaceuticals and medical devices.
Regulations applicable to life sciences organizations and logistics suppliers that produce drugs, medical devices, and medical software applications.