Shaped for your team
Requirements traceability and document control for regulated product teams, from medical device developers to the consultants who support them.
Solutions
Medical devices
Traceability, risk, and document control aligned with IEC 62304, ISO 13485, and ISO 14971.
Medical device startups
Start free, then US$35/mo per author: design controls and a live traceability matrix without an enterprise contract.
Regulatory & QA consultants
Audit-ready deliverables for independent consultants, from US$35/mo per author, with clients reviewing for free.
Quality & regulatory teams
Audit-ready documentation and live traceability, so audits become an export.
Systems engineers
Keep requirements structured and in sync with the design as it changes.
Defence programs
Requirements, hazards and verification traced and controlled, for teams working to ISO 9001, AS9100D, MIL-STD-882E and DO-178C.
See Traceable on your own documents
Import your existing requirements and see live traceability in minutes.