Introducing CURA™ The Future of Lifecycle Management in MedTech

In the world of medical technology, lifecycle management is often a complex and fragmented process. From design and development to post-market surveillance and regulatory reporting, teams are forced to navigate disconnected systems, manual workflows, and ever-evolving compliance requirements. The result? Slower innovation, higher costs, and increased risk.
That’s exactly what CURA™ was built to solve.

CURA™ is the first AI-powered, modular SaaS platform designed specifically for medical device manufacturers. It brings together every stage of the product lifecycle into one intelligent, audit-ready environment, transforming how MedTech teams operate.

At its core, CURA™ uses artificial intelligence to automate complaint handling, detect risks early, and uncover patterns that would otherwise remain hidden. It doesn’t just manage data, it learns from it. By analyzing historical complaints and manufacturing records, CURA™ identifies root causes and enables continuous improvement across your organization.

Compliance is built in. CURA™ is fully aligned with global regulatory frameworks including FDA, MDR, IMDRF, and NCIT. Whether you’re submitting reports to EUDAMED or preparing for an FDA inspection, CURA™ ensures your documentation is structured, traceable, and always ready.

The platform offers real-time dashboards and performance metrics that give you instant visibility into complaint trends, risk scores, and lifecycle KPIs. No more waiting for monthly reports or digging through spreadsheets, CURA™ puts clarity at your fingertips.

And when it comes to pricing, CURA™ breaks the mold. Instead of charging license fees or per-user costs, it uses a value-based model: you only pay a percentage of the Cost Per Closed Complaint, and only for automatically closed cases. That means no upfront risk, no wasted spend, and full access to all modules, including PMS trending, PSUR generation, adverse event reporting, and more.

The impact is measurable. CURA™ delivers up to 90% cost savings in QA and vigilance operations, a 3500% productivity boost, and 95% faster complaint processing. It empowers your QA and RA teams to focus on strategy and innovation, not paperwork.

Whether you’re a startup launching your first device or a global manufacturer managing dozens across markets, CURA™ scales with you. Its modular architecture adapts to your needs, helping you grow with confidence and control.

CURA™ isn’t just software, it’s a smarter way to manage the entire lifecycle of your medical devices. From complaint to compliance, from signal to strategy, it’s the future of MedTech operations.

Discover CURA™ and see how it transforms lifecycle management.