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Siemens Digital Industries Software › › › Verification & Validation Management

Verification & Validation Management

Verification & Validation Management

Achieve faster time to clearance by providing a single, integrated environment that ensures all medical device verification events are driven by product requirements. Whether simulation modeling and analysis or physical testing, requirements-driven product compliance can be planned and executed in the correct sequence and linked to individual tests to provide the necessary resources. Our Verification and Validation (V&V) Management solutions provide full traceability throughout the device lifecycle to complete successful product compliance.

Achieve faster time to clearance by providing a single, integrated environment that ensures all medical device verification events are driven by product requirements. Whether simulation modeling and analysis or physical testing, requirements-driven product compliance can be planned and executed in the correct sequence and linked to individual tests to provide the necessary resources. Our Verification and Validation (V&V) Management solutions provide full traceability throughout the device lifecycle to complete successful product compliance.

Verification & Validation Management

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Dramatically change the way product verification is planned, executed and managed with our solutions for Verification and Validation (V&V) Management for the medical device industry.  With these solutions, demonstrate in an auditable and efficient manner that product requirements can be achieved through successful test definition, planning, and execution.

Begin delivering superior and consistent program execution with both customers and suppliers. Manage requirements, plan and schedule verification activities, perform CAE analysis, configure and manage test articles, and confirm requirements compliance. The ability to reuse verification procedures and results will also help to reduce costs, improve product quality, and deliver programs on-time and on-budget.
Verification & Validation Management
White female professional in a lab is using an integrated labeling system on a computer screen and reviewing a document.

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Integrating labeling systems with medical device manufacturing processes

White female professional in a lab is using an integrated labeling system on a computer screen and reviewing a document.

Siemens and PRISYM ID discuss the key to optimized labeling

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솔루션 기능

Explore the key areas of this solution.

Adaptable Integrated BOM

Leverage a bill of materials management strategy that enables a single, accurate product definition for all who interact with the  device BOM.  Provide a complete, up-to-date information source which offers up-front planning, device design, development, manufacturing, service and more.

Author Manufacturing Process Plans More Efficiently

Efficiently author, analyze, manage and communicate manufacturing plans and information throughout your medical device organization.

Product Requirements Engineering

Drive the product development process by generating reports, documentation, and dashboards to manage the requirements process. Create, view and edit requirements directly from familiar Microsoft Office applications.

Project Management

Connect PLM data such as parts, documents, requirements, and more to project tasks and deliverables to ensure everyone has exactly what they need for efficient completion.  Plan, manage, and execute projects in one place, no matter how simple or complex.

Simulation Management

Efficiently manage and share CAE & system simulations to all decision-makers for a better understanding of product performance.  This knowledge helps deliver medical device innovation faster and with greater confidence.

Testing

Enhance testing processes and boost productivity and product innovation at your medical device organization.

Verification & Validation

Close the loop on requirements by capturing and associating verification and validation results with device requirements while enabling focused testing.

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