PLM for Medical Devices

Man with a performance prosthetic, running

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.

30-day free trial - Discover new possibilities in minutes

Deliver innovation faster – try PLM for Medical Devices!

Father holding his child with simulation of cochlear implant technology overlay

Experience the value of PLM for Medical Devices through a free hands-on trial. Try PLM for Medical Devices today!

A modern surgical facility

Learn More

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

Solution capabilities

Explore the key areas of this solution.

Interested in [[global-preference-center-interest-placeholder]]?

Subscribe to [[global-preference-center-interest-placeholder]] updates

Oops

We're very sorry, but we weren't able to capture your submission. Please try again.

Thanks for signing up! First time subscribing? Be sure to check your email to confirm your subscription.

Field is required A valid email address is required
Field is required Invalid value or too long