Manage complexity and improve quality by understanding the impact of changes across the medical device product lifecycle. Our systematic solutions for building-in the voice of the customer enable medical device companies to capture, manage, verify, and maintain requirements information across the development process for safer, more effective products.
Manage complexity and improve quality by understanding the impact of changes across the medical device product lifecycle. Our systematic solutions for building-in the voice of the customer enable medical device companies to capture, manage, verify, and maintain requirements information across the development process for safer, more effective products.
Capture, maintain, and deliver device requirements to everyone involved in the product development process with our requirements management solutions for medical device companies. Integrate customer needs throughout the product lifecycle by understanding the significance of change management. Our solutions offer companies insight and traceability by integrating requirements into the lifecycle. This efficient and scalable way of delivering successful products ensures all requirements are captured, linked, and maintained in the context of the specific device, thus helping mitigate the risks of non-compliance.
Explore the key areas of this solution.
Respond quickly to change from business or market disruptions and collaborate with ease with our web accessible PLM plaftorm for medical devices. Choose from flexible deployment options for fast time-to-value and low cost of ownership.
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.
