PLM for medical devices

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Our 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. Reusing, context capture, and collaboration 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 future-proofed to deliver safe, effective, and compliant devices.

Our 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. Reusing, context capture, and collaboration 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 future-proofed to deliver safe, effective, and compliant devices.

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Medical devices in an operating room

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PLM strategy for medical 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.

Integrated, multidisciplinary medical device design

Improve innovation, speed to market, and quality, enabled by:

  • Data-driven, automated processes
  • Document, design and change controls
  • Efficient cross-domain engineering collaboration
  • Integration with manufacturing & other QMS processes
  • Data-centric corrective and preventative actions (CAPA) medical device controls
A modern surgical facility

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