Download our medical device quality management datasheet to learn how Qualio:
- Arms your business with a complete, compliant eQMS for medical device quality management
- Supports and simplifies compliance with the demands of FDA 21 CFR 820, ISO 13485, the EU MDR, and more
- Digitizes and automates all areas of modern medical device quality management, from design controls to document management
Complete the form to the right to get started!
What you'll get
- Feature breakdown
Explore the core features and functionality of Qualio, and how each area of the system contributes to a holistic medical device eQMS
- Total compliance
Learn how Qualio meets the demands of ISO 13485, the medical device quality management standard, and all other national standards
- Set-up, services and more
Hear from real Qualio medical device customers, learn how we onboard and implement our software, and access more helpful resources