Medical Device Risk Management Software - Ketryx

ISO 14971-compliant medical device risk management software

Risk management is vital to build FDA-grade medical software, but error-prone manual processes leave gaps in the traceability and documentation of risks.

Managing risks effectively can be a daunting task with the constant need to ensure comprehensive documentation, adhere to regulatory standards, and track risk controls. Without a robust system in place, teams struggle with incomplete documentation, overlooked risks, and unverified controls, leading to potential compliance issues and product release delays.

Control and document every risk automatically with risk management tools

Ensure comprehensive risk control

Guarantee complete documentation of all risks and controls compliant with ISO 14971 and prevent product releases with unverified tests of risk controls (IEC 62304).

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Reduce FDA and EU MDR compliance risk

Product releases are gated by verification and validation tests of risk controls (IEC 62304).

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Save time on traceability

Save time by easily navigating across all traced items in any system with a comprehensive traceability matrix.

Read The Ultimate Guide to Requirements Traceability Matrix

Ensure QMS compliance

Ensures SOPs are followed in any connected system in the correct order.

See how Ketryx enforces your SOPs in Jira

Recapture time to focus on high-risk items

By focusing on high-risk items, you can allocate resources more effectively and ensure that all significant risks are properly controlled.

Watch webinar: Identifying Risks in AI Systems

Give risks and risk controls equivalent priority

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Check Risk Status from Any AI Tool

The Ketryx MCP Server exposes your knowledge graph through the Model Context Protocol standard, so AI tools your team already uses can query the graph directly. Engineers check risk coverage, identify traceability gaps, and verify control effectiveness without leaving their preferred AI tool.

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From Concept to Post-Market

AI-Powered Risk Management Across Every Development Phase Specialized AI Agents for High-Impact Compliance Work

Risk management doesn't stop at initial identification. It evolves throughout your product's entire lifecycle. Ketryx AI works across the TPLC, from accelerating early FMEAs to integrating post-market surveillance data.

Accelerate Risk Identification

Create comprehensive FMEAs faster with AI-generated first drafts. AI Assistant suggests failure modes based on your product type and regulatory standards, so SMEs can refine rather than starting from scratch, reducing bottlenecks and enabling earlier design decisions.

Identify and Protect Risk Controls

Know what's already controlling risk and what could. Ketryx flags existing risk controls in your requirements and design so developers don't accidentally remove them, while the AI Assistant analyzes your DHF to suggest potential new risk controls based on your design and regulatory standards.

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Complete Risk Control Verification

AI Agents identify gaps where test cases are missing. They also surface existing tests, documentation, and evidence that can verify control effectiveness. Automated traceability connects everything, while release gates prevent shipping unverified controls.

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Systematic Field Evidence Integration

Turn post-market surveillance into systematic risk management updates. AI Assistant analyzes field complaints to identify affected risks and controls, suggests whether existing mitigations remain adequate, and shows exactly which documentation needs updating. Automated traceability and version control maintain regulatory audit trails throughout.