Manage regulatory compliance through the product lifecycle.
Leaders in Life Sciences Using the Aras Platform
Mastering Design Control with Medical Device PLM
Innovation, Compliance, and Lean Product Development
Life Science companies operate in a complex, regulatory environment that demands collaboration and integration for product development. Manufacturers are often limited by legacy PLM, standalone databases, and other silos of information to track device master records, design history files, and engineer change orders, CAPA, and key project data that is often manually interchanged.
Once our users open their mind to the fact that the tools delivered by Minerva and Aras make their job so much easier, they adapt themselves quickly to the new system. With Minerva Medical Device PLM, on top of Aras Innovator, we have a nice and clean solution that is extremely easy to use, and the feedback is that everything is easier to do now. The functionalities are much more useful now, so our users are very satisfied with working with the system.
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Create digital industrial applications with our open, low-code technology. Develop any solution for engineering, manufacturing, and maintenance of complex products.
La continuité numérique
How do you own the lifecycle? One resilient platform, end-to-end, concept through service, built on shared services, low-code architecture, customizable apps, and more.
Aras’ Platform Security utilizes a combination of strategies to protect your IP and support compliance to critical regulatory programs.
Ingénierie des Exigences
Aérospatial et défense
High Tech Electronics
Step up global product development—including process automation, workflow, document control, and functionality—to support standards, quality, and regulatory compliance.
Continuously innovate smart and connected products to capture new opportunities and outpace the competition as markets shift.