Omda receives MDR certification, reinforcing commitment to quality and compliance

24 May 2024 09:30 CEST

Oslo, Norway, 24 May 2024: Today, Omda AS (“Omda”), a leading provider of
specialised software for healthcare and emergency response, announces successful
Medical Device Regulation (MDR) certification from Intertek.

This marks a significant milestone and underlines Omda’s commitment to meeting
industry standards and delivering high-quality solutions for the healthcare
professionals it serves.

MDR represents a comprehensive set of standards aimed at ensuring the safety,
efficacy, and quality of medical devices. Omda software is an integral part of
the clinical care processes of healthcare providers, who increasingly require
that their suppliers have MDR certification.

Omda CEO Sverre Flatby commented: “This MDR certification is recognised as the
highest standard in our industry and is the de facto quality stamp for medical
devices. It serves as a confirmation to our existing customers that Omda will
continue to deliver high-quality software solutions. It also opens up new growth
opportunities as we meet the formal requirements of potential customers in our
markets.”

For more information, please contact:
Helen Døcker
Chief Marketing & Communications Officer
+47 91 70 66 44
helen.docker@omda.com

About Omda
Omda is the leading provider of specialised software for healthcare and
emergency services in the Nordics with a growing presence in Europe, North
America and the Pacific region. The company has more than 500 customers in 27
countries and employs almost 300 dedicated specialists. Our highly specialised
healthcare solutions empower medical professionals and emergency responders,
enabling them to know more and work smarter. With a focus on user-centric
design, value-driven development and close working relationships with customers,
Omda delivers solutions that enhance patient safety and improve healthcare
outcomes.

For more information, visit www.omda.com
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