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

Fonctionnalités de la solution

Explore the key areas of this solution.

[[global-preference-center-interest-placeholder]] vous intéresse ?

S'abonner aux mises à jour [[global-preference-center-interest-placeholder]]

Oups

Nous sommes désolés, mais nous n'avons pas été en mesure de saisir vos informations. Veuillez réessayer.

Merci pour votre inscription ! C’est votre première inscription ? N’oubliez pas de répondre à l’e-mail que nous vous avons fait parvenir pour confirmer votre inscription.

Champ obligatoire Une adresse e-mail valide est requise
Champ obligatoire Valeur non valable ou trop longue
Champ obligatoire Une adresse e-mail valide est requise