Innovation and collaborative, synchronized program management for new programs
Explore the key areas of this solution.
Globally centralize, manage, and distribute manufacturing information while orchestrating all related processes and activities within a product lifecycle context, under full configuration and change control.
Participate in all aspects of a controlled medical device development process with our product configuration solutions. Subject all device requirements to the same lifecycle processes, variants, workflows, and access controls for optimum efficiency.
Provide cross-domain requirements traceability to ensure medical device organizations successfully develop mechanical and software-driven electronic systems.
Develop complex medical devices through integrated planning and execution in a single, integrated system. Collaborate and communicate key information among interdisciplinary teams to shorten time to market and enable early-stage issue detection.
Quickly and easily create standard requirement reports, dashboard views, and device specifications including requirements, traceability, verification, variation, status, and impact analysis for complete visibility into the entire device development process.
Link device requirements to all aspects of the product definition including: specifications, Bill of Materials, program/project tasks, test cases, 1D and 3D models, manufacturing processes, and more. This allows insight into change propagation in ways never before possible.
Embed requirements across the medical device lifecycle with our requirements capture and reuse capabilities. Tie requirements to standard product management processes, including change and workflows, for inclusion in standard reporting and dashboards.
Participate in standard change management practices either as a requirements change process or at the product change level. Include device modifications within global change planning to eliminate working from stale requirements.
Effectively gather, author, approve and manage requirements for complex systems across the entire medical device lifecycle.
Participate in all aspects of a controlled medical device development process with our product configuration solutions. Subject all device requirements to the same lifecycle processes, variants, workflows, and access controls for optimum efficiency.
Provide cross-domain requirements traceability to ensure medical device organizations successfully develop mechanical and software-driven electronic systems.
Link device requirements to all aspects of the product definition including: specifications, Bill of Materials, program/project tasks, test cases, 1D and 3D models, manufacturing processes, and more. This allows insight into change propagation in ways never before possible.
Participate in standard change management practices either as a requirements change process or at the product change level. Include device modifications within global change planning to eliminate working from stale requirements.