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.
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