Qaralogic
  • Regulatory & Quality Consulting
    • US Market
    • Canadian Market
    • EU Market
    • Global Markets
  • Our Team
  • Resources
  • Contact
  • Book a Call
  • Regulatory & Quality Consulting
    • US Market
    • Canadian Market
    • EU Market
    • Global Markets
  • Our Team
  • Resources
  • Contact
  • Book a Call

EU MDR

EU-MDR workshop

Published: Nov 20, 2021 by Hasnaa Fatehi, PhD Read Time: 1m

Portrait of Hasnaa Elhaddad

About the author

Hasnaa Fatehi, PhD


Hasnaa has two decades of MedTech experience including clients such as Procter & Gamble, Stryker and LivaNova. Her academic background includes a BSc in Mechanical Engineering, an MSc in Biomedical Engineering with a focus on Ultrasound imaging, and a PhD in Systems Biology - giving her a technical fluency in device design and risk which can be critical for complex and detailed compliance systems.

Qaralogic

Regulatory clarity. Global reach.

Book a call

© 2026 Qaralogic Consulting Inc.

Join the Regulatory Raconteur

Stay up to date with the regulatory landscape

Each issue of the Qaralogic newsletter breaks down a recent regulatory update or medical device compliance trend from the US, EU, and Canada, and what it actually means for your product roadmap. You'll also get practical guidance on submissions, QMS, and ISO 13485, the kind of insight we normally reserve for client engagements.


  • RAC Devices
  • RAPS Member
  • BSI ISO 13485 Lead Auditor
  • Medtech Canada