See how a neurovascular technology startup replaced manual requirements tracking with Live Traceability™, automated test integration, and regulatory reporting using Jama Connect.
Developing Software as a Medical Device (SaMD) for complex neurovascular procedures requires precise requirements management, documented verification, and alignment with medical device standards.
For Sim&Cure, managing requirements and traceability in Word and Excel made it difficult to track changes, coordinate teams, and prepare regulatory documentation. The company needed a more structured approach that could support its development process as it grew.
After evaluating eight platforms, Sim&Cure selected Jama Connect for its configurable regulatory reporting, end-to-end traceability, and open API.
