Product

What is Ketryx?

Connected Lifecycle Management platform for regulated medical applications.

AI/ML in Medical Devices

Rapidly accelerate AI/ML software development and deployment, while staying compliant.

SaMD and Connected Devices

Reduce the complexity, time, and cost of building SaMD (Software as a Medical Device) applications.

Transform Jira into a validated, compliant platform for medical device development.

AI for Life Sciences (GxP)

Reduce the complexity, time, and cost of GxP validation for your application.

Component Reuse

Accelerate development and reuse components through a system of systems architecture.

Traceability to Automated Tests

Automatically trace automated tests in Git to requirements in Jira.

Multifunction Devices

Release device and non-device functions independently with a system of systems architecture.

Watch a short recorded demo

Automate arduous tasks across your toolchain with safety-critical AI agents that keep a human in the loop.

Automatically create a real-time requirements traceability matrix by connecting items, risks, code, and tests from all your systems.

Automatically compile all requirements, design inputs, outputs, and tests into a configurable and submission-ready design history file (DHF).

Enforce your QMS to ensure your team is following SOPs exactly as you've defined them.

See a single consolidated view of your open-source supply chain directly from your source code.

Requirements Management

Manage and trace requirements across connected systems like Jira.

Risk Management

Control and document every risk automatically in a 14971-compliant way.

Navigate compliance confidently with an eQMS that's interoperable with all your favorite tools.

Watch a short recorded demo

Enforce your QMS procedures, prevent process deviation, and ensure your software is audit-ready 100% of the time throughout the SDLC.

Keep your developers working in their preferred DevTools while maintaining compliance and traceability.

Reduce your documentation burden by 90% and release your AI products faster.

Watch a short recorded demo

What is Ketryx?

Connected Lifecycle Management platform for regulated medical applications.

Use Cases

AI/ML in Medical Devices

Rapidly accelerate AI/ML software development and deployment, while staying compliant.

SaMD and Connected Devices

Reduce the complexity, time, and cost of building SaMD (Software as a Medical Device) applications.

Transform Jira into a validated, compliant platform for medical device development.

AI for Life Sciences (GxP)

Reduce the complexity, time, and cost of GxP validation for your application.

Component Reuse

Accelerate development and reuse components through a system of systems architecture.

Traceability to Automated Tests

Automatically trace automated tests in Git to requirements in Jira.

Multifunction Devices

Release device and non-device functions independently with a system of systems architecture.

Watch a short recorded demo

Capabilities

Automate arduous tasks across your toolchain with safety-critical AI agents that keep a human in the loop.

Automatically create a real-time requirements traceability matrix by connecting items, risks, code, and tests from all your systems.

Automatically compile all requirements, design inputs, outputs, and tests into a configurable and submission-ready design history file (DHF).

Enforce your QMS to ensure your team is following SOPs exactly as you've defined them.

See a single consolidated view of your open-source supply chain directly from your source code.

Requirements Management

Manage and trace requirements across connected systems like Jira.

Risk Management

Control and document every risk automatically in a 14971-compliant way.

Navigate compliance confidently with an eQMS that's interoperable with all your favorite tools.

Watch a short recorded demo

Function

Enforce your QMS procedures, prevent process deviation, and ensure your software is audit-ready 100% of the time throughout the SDLC.

Keep your developers working in their preferred DevTools while maintaining compliance and traceability.

Reduce your documentation burden by 90% and release your AI products faster.

Watch a short recorded demo

Case Studies

Learn how AI-powered radiology company DeepHealth accelerated product development with Ketryx

Discover how AI/ML-enabled cardiovascular MedTech company HeartFlow reduced complexity by 90% with a system of systems

See how AI-powered nutrition platform Nutrino reduced SBOM documentation time by 90%

Learn how Beacon Biosignals reduced their release cycle to two weeks for AI/ML products

Discover how AI pathology company Aignostics stopped copying and pasting and accelerated their release cycle time

Explore how Foresight Diagnostics accelerated their documentation cycle by 5x

See how AI-enabled cardiovascular MedTech company Vektor Medical reduced documentation cycle time by 60%

See how Oui Therapeutics unified and accelerated their software development lifecycle

“The Ketryx software enables us to scale our innovation with quality through a single streamlined software development lifecycle, helping us expedite releases.”

Sham Sokka

Chief Operating and Technology Officer for Digital Health

"Ketryx is becoming an intrinsic part of every piece of software we build. It’s not another tool we have to use on the side to be compliant with standards; it’s just a natural way of developing high-quality software with excellence."

Helmut Hoffer von Ankershoffen

Senior VP Product and Engineering

"Vektor Medical has been through three audits, including one from a leading notified body in 2024. All auditors were amazed by the level of detail, linkage and control that is built into Ketryx. The auditors were especially impressed by the trace matrix dashboard and risk management module. Ketryx is an efficient and compliant solution for medical device software development."

Mihir Naik

Senior Director, Quality

“Ketryx empowered Nutrino to accelerate the adoption of OTS software and SOUP, ensuring confidence in our ability to proactively identify high-risk components and address potential issues early in the premarket submission cycle. This streamlined SDLC process has enabled us to deliver innovative and safe diabetes solutions much more rapidly.”

Chen Weitz

Senior Engineering Director

"I used a traditional ALM in the past and it didn’t have the traceability I needed, especially tracing from my test executions and results. It also created duplicate work since I needed to go update my work there every time I completed a task. Ketryx updates itself as I’m working in Jira and GitHub. This tighter integration into our current tools helps us be more productive and release faster."

Aaron Berlin

SVP Development and Engineering

“Ketryx supports our system of systems architecture really easily out of the box. We were able to migrate our monolithic ecosystem into a single project and break it down into a desired state just within a couple of days. Ketryx delivered that because it was designed to scale. That was a huge plus.”

Emre Gültürk

VP of Regulatory Affairs and Quality Systems

“Ketryx has allowed us to channel our hardware and software engineers’ existing set of development, testing, and documentation practices directly into the generation of compliant documentation with minimal additional burden. This has allowed us to remain agile while delivering high-quality products.”

Alexander Chan

VP of Analytics and Machine Learning

“Overall we’ve been very happy relative to our previous workflow. Ketryx lets us get a lot more granular and more specific in terms of defining the configuration items. It maps much better onto our software development workflow and processes.”

Alec Winograd

VP of Engineering

Pricing

Resources

Access Ketryx's extensive product documentation.

Learn about regulated medical device software development.

Support and FAQs

Customers submit tickets here for all product needs.

Hear from experts on medical device software development.

Take a deep dive into regulated software development.

About

Learn the origin story of Ketryx and how we got to where we are today.

Understand why regulated software teams choose Ketryx.

Learn about our team and opportunities to join us.

See recent press about Ketryx's work with life sciences teams.

See our compliance with international standards

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Book a Demo Preview Ketryx

Get Started 

In-person events

American Medical Device Summit 2025

October 27, 2025

,

9:00 am

EST

Date and time TBD

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Develop fast. Stay compliant.

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