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Ease your ISO 13485 certification process with Scilife

Dive deeper into critical elements of ISO 13485 compliance and discover Scilife's top five capabilities:

  • Ensure compliance and prepare your organization for EU MDR audit
  • Improve your document management and guarantee data integrity
  • Align your quality management processes with ISO requirements
Scilife eQMS for Medical Devices | Scilife

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Scilife solutions for 
medical devices

In this free session, Angel Buendía (Knowledge Manager) and Jordi Ametller (Product Specialist Lead) will show you how Scilife can help you embark your ISO 13485 certification journey smoothly. 


What you’ll learn in this session

In this session, we’ll see a practical demonstration of how to: 

  • Streamline document management for ISO 13485 compliance.
  • Ensure data integrity and compliance with ISO 13485 record-keeping standards.
  • Master event documentation for ISO 13485 compliance.
  • Implement effective CAPAs per ISO 13485 standards.
  • Meet ISO 13485 requirements for vendor qualification and audit management.



Angel Buendia

Knowledge Manager
at Scilife


Jordi Ametller

Product Specialist Lead
at Scilife