Innovazione e gestione dei programmi sincronizzata e collaborativa per i nuovi programmi
Siemens Product Lifecycle Management (PLM) for Medical Devices is an integrated cloud-based product development system that helps manufacturers overcome product complexity and the burdens of industry regulation. Through re-use, context capture, and collaboration, it helps improve visibility and traceability through digitalization while reducing costs and compliance risks.
This medical device lifecycle software integrates disciplines to drive optimal product functionality. As demands change, it's futureproofed to deliver safe, effective, and compliant devices.
Siemens Product Lifecycle Management (PLM) for Medical Devices is an integrated cloud-based product development system that helps manufacturers overcome product complexity and the burdens of industry regulation. Through re-use, context capture, and collaboration, it helps improve visibility and traceability through digitalization while reducing costs and compliance risks.
This medical device lifecycle software integrates disciplines to drive optimal product functionality. As demands change, it's futureproofed to deliver safe, effective, and compliant devices.
PLM for Medical Devices helps manufacturers develop devices efficiently and increase their competitive advantage in the face of market and regulatory pressures.
Comprehensive PLM software provides complete design control digitalization, integration to design and document authoring apps, and workflow-based change control and CAPA processes resulting in high-value, optimized devices.
Automate, standardize, and enhance your product development process. Manage product variations according to regional needs. Realize complete traceability from risks and requirements to V&V testing to DHF/DMR records and regulatory submissions. Maintain a digital system of record that’s web-accessible, secure, and compliant.
Improve innovation, speed to market, and quality, enabled by:
Explore the key areas of this solution.
SaaS PLM, for faster time to value and lower cost of ownership, or on-premise.
Workflows digitalize, globalize, harmonize and accelerate your capstone processes.
Configure and control your regional device variations using bill of material constructions.
Template-driven, re-usable, configurable regulatory record and document collections.
Integrated document authoring, via PLM embedded in your Office and Adobe apps.
Integrated 3D design system via PLM embedded in your ECAD apps.
Integrated 3D design system, via PLM embedded in your MCAD apps.
Traceability from risk files and analyses to device and manufacturing requirements, to V&V testing.
With medical devices becoming more complex and regulatory oversight becoming stricter, it is difficult for manufacturers to deliver products effect...
To bring your products to market quickly, product design and development must stay flexible. Healthcare providers and patients require increased pr...