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Kinaxis Selected to Accelerate Technical Operation Transformation of Major Pharmaceutical Company

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Kinaxis® Inc. , provider of RapidResponse®, the recognized leader in digital supply chain management for concurrent planning.

Announced that the Swiss-based pharmaceutical company, Novartis AG,  has selected Kinaxis RapidResponse as their new supply chain planning system for their global TechOps organization, as part of a wider supply chain transformation initiative. Kinaxis will help Novartis enable next-generation planning capabilities to improve speed, efficiency and collaboration for more informed decision-making.

Novartis products reach nearly one billion people globally every year through a supply chain that includes thousands of suppliers and extends into most countries. Using Kinaxis, Novartis aims to gain end-to-end supply chain visibility, respond more quickly to changing market demands, improve inventory management and drive down costs. Once fully implemented, Kinaxis will help Novartis drive planning standardization across all divisions of the organization and use advanced analytics to help manage the complexity of business planning.

About Kinaxis Inc.
As the recognized leader in digital supply chain management for concurrent planning, Kinaxis is helping organizations around the world revolutionize their supply chain planning. Kinaxis RapidResponse, our cloud-based supply chain management software, connects your data, processes and people into a single harmonious environment. With a consolidated view of the entire supply chain, you can plan expected performance, monitor progress and respond to disconnects when reality hits. RapidResponse lets you know sooner and act faster, leading to reduced decision latency, and improved operational and financial performance. We can prove it. From implementation to expansion, we’re here to help our customers with every step of their supply chain journey.

Latest stories

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Establishing a robust framework for regulatory success requires moving beyond fragmented information silos toward a unified, digital-first approach. Comprehensive oversight of the pharmaceutical lifecycle depends on the ability to transform raw information into actionable insights, ensuring that every data point contributes to a larger narrative of safety and efficacy. By prioritizing specialized platforms that aggregate and organize complex information, organizations can achieve a level of transparency that satisfies the most stringent global standards while fostering a culture of continuous improvement.

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Centralizing expert-verified toxicological datasets is now a critical requirement for modern pharmaceutical facilities operating under stringent global regulations. By transitioning from generic cleaning limits to precise Health-Based Exposure Limits derived from high-quality platforms, manufacturers ensure that cleaning validation protocols are scientifically sound and audit-ready. This approach integrates rigorous toxicological risk assessment into the broader contamination control strategy, safeguarding patient health while optimizing multi-product manufacturing efficiency and regulatory compliance.

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Advancing Quality 4.0 Through Centralized Drug Knowledge 

Implementation of a unified data framework serves as the catalyst for modernizing pharmaceutical production, bridging the gap between legacy processes and intelligent automation. By consolidating disparate data streams into a cohesive repository, organizations achieve unprecedented visibility into critical quality attributes and process parameters. This transformation facilitates proactive risk mitigation and ensures that Good Manufacturing Practices are maintained through high-fidelity insights rather than retrospective analysis, ultimately fostering a culture of continuous improvement and operational excellence.

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