Custom Software for Medical Device Companies

Specialized algorithms

Seamless integration with hardware components

Supports unique workflows

End-to-end encryption

Reduces risks of cyberattacks

Custom APIs for interoperability

Easy updates that doesn’t disrupt operations

Faster prototyping for FDA-cleared devices

Interoperability Issues

Fragmented data formats, proprietary protocols, and inconsistent integration with hospital systems and EHRs create barriers that slow down workflows, create data silos, and compromise clinical efficiency.

User Experience (UX) in a Clinical Setting

Its hard to balance simplicity with functionality, especially on constrained hardware like embedded systems.

Cost and Talent Constraints

Many developers are unfamiliar with regulatory-grade documentation and design controls.

Cybersecurity and Data Privacy

Its a challenge to keep up with evolving threats while staying compliant with laws like HIPAA, GDPR, and new cybersecurity frameworks (e.g., FDA’s premarket cybersecurity guidance).

Product Discovery

Refine your existing product concept before development to ensure your device addresses real clinical needs and complies with regulatory standards, reducing potential risks. We offer a structured discovery phase where we conduct market research, define product requirements, and validate ideas with key stakeholders.

Software Modernization

Upgrade and enhance your existing software to meet current industry demands. We can help you refactor outdated code, integrate new features, and ensure compatibility with modern hardware and software ecosystems, minimizing disruptions and maximizing long-term performance.

End-to-end Software Development

We help companies to improve their products, deliver better patient outcomes, and stay competitive. Deliver precise diagnostics, personalized treatment plans, and advanced monitoring, which will lead to improved patient outcomes.