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Home / Resources / Blog /

Blog

Why “Free” DICOM Viewers Are Not Sustainable — and Why OsiriX Is Different

February 14, 2026
Not all DICOM viewers are created equal. Many “free” or open-source forks of the original OsiriX have become unstable and unvalidated — putting medical practices at risk. OsiriX MD stands apart: continuously developed, FDA-cleared, CE-marked, and fully supported. In medical imaging, sustainability means reliability — and OsiriX delivers both.
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How OsiriX Enhances Veterinary Imaging: A Real-World Use Case

December 8, 2025
Veterinary imaging is evolving fast — and OsiriX MD is leading the way. Discover how a veterinary diagnostic center uses OsiriX to analyze complex CT and MRI scans, improve collaboration, and enhance animal care. With its fast performance, stunning 3D visualization, and intuitive tools, OsiriX is redefining efficiency in veterinary radiology.
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How OsiriX Empowers Cardiac Imaging: A Real-World Use Case

November 24, 2025 - by Antoine Rosset
In today’s fast-paced medical environments, speed and precision in imaging can transform patient care. Discover how a cardiology team uses OsiriX MD to streamline cardiac CT analysis, reduce diagnosis time, and enhance collaboration. From stunning 3D heart visualizations to seamless PACS integration, this real-world case study shows why OsiriX remains the go-to solution for clinicians who demand performance and accuracy.
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OsiriX
OsiriX
  • Overview
  • For Mac
  • For Mobile
  • Solutions
  • Institutions
  • Patients
  • OsiriX Study Sharing
Support
  • Getting Started
  • Tutorials
  • Help Center
  • Premium Membership
  • FAQ
  • OsiriX Cloud FAQ
  • Knowledge Base
Resources
  • Technical Sheet
  • PACS
  • RIS Integration
  • DICOM Image Library
  • Plugins
  • Plugins Development
  • Blog
About
  • Company
  • Story
  • Ambassadors
  • Partners
  • Our Users
  • References
  • Contact
OsiriX Copyright © 2026 Pixmeo | Terms of use
OsiriX MD is cleared by the FDA, as a Class II Medical Device, for diagnostic imaging in medicine
OsiriX MD complies with European Directive 93/42/ EEC concerning medical devices. Under this directive, it is regarded as a Class IIa product. Notified Body: DQS Medizinprodukte GmbH, 0297