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Improving Medical Device Quality and Compliance with SaaS PLM

Improving Medical Device Quality and Compliance with SaaS PLM

 

Improving Medical Device Quality and Compliance with SaaS PLM

Medical device manufacturers face rising pressure to deliver safe, compliant products while managing growing complexity across design, risk, and regulatory processes. This eBook explains how a SaaS-based PLM approach helps teams replace siloed quality systems with a connected, data-driven foundation. It shows how Siemens PLM for Medical Devices supports quality-by-design while improving traceability, collaboration, and execution across the full product lifecycle.

What You’ll Learn

  • How SaaS PLM centralizes quality, risk, and design data into a single system of record
  • How integrated quality process management supports CAPA, change control, DHF, and DMR requirements
  • How digital risk and requirements management aligned to ISO 14971 improves traceability and consistency
  • How cloud-based PLM enables cross-domain collaboration across systems, mechanical, electrical, and software teams

    • Why It Matters

  • Reduces compliance risk by maintaining complete traceability across design, quality, and regulatory artifacts
  • Improves product quality and speed to market by replacing document-centric processes with connected workflows
  • Scales quality operations globally with a flexible SaaS platform that adapts to evolving regulations and product portfolios

    • Download the full eBook to learn how SaaS PLM helps medical device teams deliver high-quality, compliant products more efficiently.

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