Automate your software compliance
Get rid of software bottlenecks. Ultralight helps medical device software teams implement engineering best practices while simplifying compliance to IEC 62304 and other gold standard frameworks.
IEC 62304
ISO 13485
ISO 14971
Documentation-in-Code
Increase efficiency and bridge the gap between engineering and quality
Automate documentation and release faster
Give engineering the tools they need to document efficiently. Enable documentation-in-code for better traceability and reduce non-compliance and documentation drift. Eliminate manual processes, and speed up your releases by getting rid of bottlenecks.
Set up with your existing tools with a few lines of code
Keep using whatever tools you use and set up with a few lines of code, and collect data automatically in Ultralight. Report test protocols, test results and keep your Design History File up to date seamlessly.
Cybersecurity
Comply with ever-changing cybersecurity requirements
Easily manage cybersecurity risk with a few clicks
Manage your software supply chain using Ultralight's Software Bill of Materials (SBOM) management to comply with FDA requirements.
Understand your vulnerability posture
Ultralight will automatically scan your SBOMs to get vulnerability information, and make sure you know what your SOUP and OTS vulnerabilities are.
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