Inovação e gerenciamento de programa sincronizado e colaborativo para novos programas
Developing complex, long-life products are the key to success in the medical device market. Providing the opportunity to increase and stabilize revenue and profit streams while securing customer loyalty is paramount given the competitive nature of the industry.
As such, this requires greater understanding of product performance and planning for service during device development. By incorporating service functionality within the lifecycle environment used for product development, it allows closer collaboration. This in turn yields better, safer products, better service, and a better bottom line.
Our as-maintained solutions provide an environment for medical device companies to manage service knowledge and product knowledge using the same security and advanced core functionality. This unified approach aligns the digital twin of the product with the digital twin of physical product to close the loop on product performance. In this way, companies can manage the physical configuration of products to support test, recall, and maintenance throughout the entire history of parts and product.
Developing complex, long-life products are the key to success in the medical device market. Providing the opportunity to increase and stabilize revenue and profit streams while securing customer loyalty is paramount given the competitive nature of the industry.
As such, this requires greater understanding of product performance and planning for service during device development. By incorporating service functionality within the lifecycle environment used for product development, it allows closer collaboration. This in turn yields better, safer products, better service, and a better bottom line.
Our as-maintained solutions provide an environment for medical device companies to manage service knowledge and product knowledge using the same security and advanced core functionality. This unified approach aligns the digital twin of the product with the digital twin of physical product to close the loop on product performance. In this way, companies can manage the physical configuration of products to support test, recall, and maintenance throughout the entire history of parts and product.
Capture issues with medical devices and manage corrective and preventative actions to improve both product and product service with our digital as-maintained solutions. By managing the authoring, approval, and access of documents associated with product and service, your medical device company can effectively ensure device quality and conformance from design through to production.
Furthermore, analyze service and product data to establish trends in performance for both with comprehensive dashboards and reports. Create innovative, sustainable products and enable material-driven product design for products and processes which will meet, if not exceed, specification requirements and compliance mandates. The end result will yield more innovative devices which adhere to all necessary regulations and employ a lifecycle process which supports these goals on a continual basis.
Explore the key areas of this solution.
Provide a common source of BOM information across your med-tech organization, whether basic or advanced, for greater flexibility so you can exceed market demand for more innovative and varied product offerings.
Make smart business decisions with full visibility into the device development process thanks to a single source of reporting and analytics information. Create new reports via self-service tools to quickly gain an understanding of your products and processes.
Optimize product change management processes at your medical device company for a clear understanding of the data, people, and processes impacted by change. This enables you to effectively plan, leverage flexible change processes to meet specific needs, and provide full device change traceability.
Enhance product service understanding through 3D display of parts and assemblies with our real-time digital mockup tools. Detect and resolve design issues earlier with visualization mockup capabilities and distribute universally viewable information to team members across your entire medical device organization.
Automate any PLM process and create workflows that build-in your business logic. Define standard process templates to enforce best practices to eliminate errors, access instant status updates, device history files, and audit trails to ensure complete control and visibility into the device lifecycle processes.
Help all teams at your med-tech company create specifications, analysis reports, illustrations, test results, and technical publications that are aligned with product changes. This will reduce the time and cost of development, while improving document accuracy and effectiveness.
Ensure product quality across the entire device lifecycle with our quality issue management and corrective and preventive action (CAPA) solutions. Capture complaints, defects, and non-conformance with product engineering, production planning, simulation, and validation tools for complete quality management.
Efficiently manage the materials used in your medical devices so your company can create innovative, sustainable products. Our holistic materials management solution provides data throughout your enterprise supporting all aspects of the product lifecycle.
Allocate requirements to various downstream functions while generating reports, documentation, and dashboards to manage the requirements process. Create and edit requirements directly from familiar applications to enable smart development processes across the entire device lifecycle.
Make smart business decisions with full visibility into the device development process thanks to a single source of reporting and analytics information. Create new reports via self-service tools to quickly gain an understanding of your products and processes.
Optimize product change management processes at your medical device company for a clear understanding of the data, people, and processes impacted by change. This enables you to effectively plan, leverage flexible change processes to meet specific needs, and provide full device change traceability.
Enhance product service understanding through 3D display of parts and assemblies with our real-time digital mockup tools. Detect and resolve design issues earlier with visualization mockup capabilities and distribute universally viewable information to team members across your entire medical device organization.
Automate any PLM process and create workflows that build-in your business logic. Define standard process templates to enforce best practices to eliminate errors, access instant status updates, device history files, and audit trails to ensure complete control and visibility into the device lifecycle processes.
Help all teams at your med-tech company create specifications, analysis reports, illustrations, test results, and technical publications that are aligned with product changes. This will reduce the time and cost of development, while improving document accuracy and effectiveness.
Ensure product quality across the entire device lifecycle with our quality issue management and corrective and preventive action (CAPA) solutions. Capture complaints, defects, and non-conformance with product engineering, production planning, simulation, and validation tools for complete quality management.
Allocate requirements to various downstream functions while generating reports, documentation, and dashboards to manage the requirements process. Create and edit requirements directly from familiar applications to enable smart development processes across the entire device lifecycle.