Traceable

Traceable records the design documentation behind a quality product: requirements and design inputs, risk assessments, test protocols and reports, and the trace links that connect them. Every document is under control, with review, approval and e-signature. It is built for teams who must show their product is safe and works as intended: medical devices, IVD, software as a medical device, defence and aerospace, and high-quality consumer software and hardware. It is not tied to any one standard, and supports the documentation for ISO 13485, ISO 14971, IEC 62304, ISO 9001, AS9100D, ISO/IEC/IEEE 15288, DO-178C and MIL-STD-882E, among others. With this connector, Claude works in your Traceable account the way you do, with your permissions. It can: - Map a project and show how its documents trace to each other - Read documents and draft new ones from your organisation's templates - Write requirements into ID grids and create trace links - Record test results and attach evidence - Search the Reference Library, cite standards and add glossary terms - Upload images into documents - Plan documents on a project's Design Phases board or quality system diagram Built for controlled work: - Claude acts as you, so a read-only role stays read-only - Read and write tools are labelled separately, so you can let Claude read freely and approve every change - Changes land in drafts. Publishing, review, approval and e-signature stay with people - Every change is recorded in the audit trail under your name, and by default a person must accept agent-written rows before a document can be published Requires a Traceable account with MCP access enabled by an organisation admin. Included on every plan, with rate limits on Free.