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Product
Use Cases
Capabilities
Function
Integrations
What is Ketryx?
AI-native compliance for regulated medical applications
Read more
Solutions
Capabilities
Function
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.
Jira for 62304
Transform Jira into a validated, compliant platform for medical device development.
System of Systems
Accelerate development and reuse components through a system of systems architecture.
AI Governance for Life Sciences
Reduce the complexity, time, and cost of GxP validation for your application.
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.
Hardware-Software Products
Unify compliance and accelerate development across mechanical, electrical, and software teams
Watch a short recorded demo
AI Agents
Automate arduous tasks across your toolchain with safety-critical AI agents that keep a human in the loop.
Compliance in your AI Tools
Real-time compliance context embedded directly into your IDE and LLM via MCP
SBOM Management
See a single consolidated view of your open-source supply chain directly from your source code.
Traceability
Automatically create a real-time requirements traceability matrix by connecting items, risks, code, and tests from all your systems.
Documentation
Automatically compile all requirements, design inputs, outputs, and tests into a configurable and submission-ready Design and Development File.
Enforcement
Enforce your QMS to ensure your team is following SOPs exactly as you've defined them.
AI SDLC Transformation
Accelerate your AI maturity, guided by our experts
Requirements Management
Manage and trace requirements across connected systems like Jira.
Risk Management
Control and document every risk automatically in a 14971-compliant way.
eQMS
Navigate compliance confidently with an eQMS that's interoperable with all your favorite tools.
AI Change Impact Assessment
Apply AI to automate change impacts across your Design and Development File, reducing manual effort and increasing trust.
AI Assistant
Generate compliant artifacts, analyze traceability, and answer QMS questions using your real project context.
Watch a short recorded demo
QA / RA
Enforce your QMS procedures, prevent process deviation, and ensure your software is audit-ready 100% of the time throughout the SDLC.
Dev / R&D
Keep your developers working in their preferred DevTools while maintaining compliance and traceability.
AI/ML Leaders
Reduce your documentation burden by 90% and release your AI products faster.
Systems Engineering
Manage architecture and monitor change impact across the total product lifecycle
Watch a short recorded demo
What is Ketryx?
AI-native compliance for regulated medical applications
Read more
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.
Jira for 62304
Transform Jira into a validated, compliant platform for medical device development.
System of Systems
Accelerate development and reuse components through a system of systems architecture.
AI Governance for Life Sciences
Reduce the complexity, time, and cost of GxP validation for your application.
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.
Hardware-Software Products
Unify compliance and accelerate development across mechanical, electrical, and software teams
Watch a short recorded demo
Capabilities
AI Agents
Automate arduous tasks across your toolchain with safety-critical AI agents that keep a human in the loop.
Compliance in your AI Tools
Real-time compliance context embedded directly into your IDE and LLM via MCP
SBOM Management
See a single consolidated view of your open-source supply chain directly from your source code.
Traceability
Automatically create a real-time requirements traceability matrix by connecting items, risks, code, and tests from all your systems.
Documentation
Automatically compile all requirements, design inputs, outputs, and tests into a configurable and submission-ready Design and Development File.
Enforcement
Enforce your QMS to ensure your team is following SOPs exactly as you've defined them.
AI SDLC Transformation
Accelerate your AI maturity, guided by our experts
Requirements Management
Manage and trace requirements across connected systems like Jira.
Risk Management
Control and document every risk automatically in a 14971-compliant way.
eQMS
Navigate compliance confidently with an eQMS that's interoperable with all your favorite tools.
AI Change Impact Assessment
Apply AI to automate change impacts across your Design and Development File, reducing manual effort and increasing trust.
AI Assistant
Generate compliant artifacts, analyze traceability, and answer QMS questions using your real project context.
Watch a short recorded demo
Function
QA / RA
Enforce your QMS procedures, prevent process deviation, and ensure your software is audit-ready 100% of the time throughout the SDLC.
Dev / R&D
Keep your developers working in their preferred DevTools while maintaining compliance and traceability.
AI/ML Leaders
Reduce your documentation burden by 90% and release your AI products faster.
Systems Engineering
Manage architecture and monitor change impact across the total product lifecycle
Watch a short recorded demo
Integrations
Case Studies
Learn how Meta Reality Labs builds regulated medical products without sacrificing engineering velocity.
See how Flo Health, with 430M users, transitioned to regulated development in just 90 days
Learn how AI-powered radiology company DeepHealth accelerated product development with Ketryx
How This AI-Powered Medical Software Company Reduced SBOM Documentation Time by 90%
Discover how AI/ML-enabled cardiovascular MedTech company HeartFlow reduced complexity by 90% with a system of systems
Learn how an AI-driven diagnostics company transformed change impact assessment
Learn how Beacon Biosignals reduced their release cycle to two weeks for AI/ML products
Learn how a Top 5 MedTech company assessed vulnerabilities 80% faster
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%
Learn how an Enterprise IVD company accelerated end-to-end release cycles by 85%
“Ketryx AI is the most scalable approach we’ve used for regulated product development. It lets our teams make frequent, safe changes while staying continuously audit-ready, without relying on linear headcount growth or stopping teams for compliance exercises.”
Lucas Fernandez
Director of Medical Devices
"Ketryx gave us a scalable way to manage product cybersecurity risk. We’re running assessments more frequently, prioritizing the right issues, and improving our overall security posture without increasing effort."
Director of Product Security
"Delivering quickly is core to our mission because faster releases mean better health outcomes for our users. Ketryx is the only partner we found that gave us the ability to maintain our velocity while achieving medical-grade quality.”
Roman Bugaev
CTO
“We’re excited about how Ketryx helps us improve our overall pace of release. With Ketryx’s AI, we’ve transformed our multi-week manual process of change impact analysis into less than an hour.”
CTO
“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
Industries
Physical AI
IEC 61508 & ISO 9001 for functional safety
Medical Devices
FDA, MDR, ISO 13485 aligned development
Robotics
IEC 61508 compliant autonomous systems
Automotive
ISO 26262 & ASPICE aligned lifecycles
Aerospace
DO-178C, DO-254, ARP4754A assurance
Defense
CMMC, MIL-STD-882E & 498 aligned mission systems
Nuclear Energy
IEC 61513 & 60880 compliant digital I&C modernization
Pricing
Resources
Documentation
Access Ketryx's extensive product documentation.
Blog
Learn about regulated medical device software development.
Support and FAQs
Customers submit tickets here for all product needs.
Webinars
Hear from experts on regulated product development.
In-Person Events
Network with peers in life science and the Ketryx team
White Papers
Take a deep dive into regulated software development.
Demo Video Library
See the Ketryx platform in action
About
Company
Learn the origin story of Ketryx and how we got to where we are today.
Why Ketryx
Understand why regulated software teams choose Ketryx.
Careers
Learn about our team and opportunities to join us.
Newsroom
See recent press about Ketryx's work with life sciences teams.
Certifications
See our compliance with international standards
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Free Webinars
The Future of Change Management for Cloud-Based AI/ML Medical Software
60
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Webinar Resources for change management and compliance
The latest changes to the FDA’s new premarket submission guidance
Simplifying 510K Submissions with FDA’s eSTAR Program
PATCH Act: How to comply in 2023 & Beyond
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