EU MDR software datasheet

Download our EU MDR compliance software datasheet to learn how Qualio:


  • Arms your business with a complete, EU-compliant eQMS for medical device quality management

  • Supports and simplifies compliance with Regulation (EU) 2017/745, more commonly known as the Medical Device Regulation (MDR)

  • Digitizes and automates all areas of medical device quality management, from design controls to document management

Complete the form to the right to get started!
What you'll get:

1. Feature breakdown

Explore the core features and functionality of Qualio, and how each area of the system contributes to a holistic medical device eQMS
2. Complete EU MDR compliance

Learn how Qualio helps your business meet the demands of each section, annex and chapter of the Medical Device Regulation
3. 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