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9 May 2025 – London, UK (NTSE ‘DAVA’) Endava is proud to announce the receipt of the ISO 13485:2016 certification for our first medical device, marking a key achievement in our commitment to quality and innovation. 

 

Achieving this certification not only highlights our dedication to patient safety, product quality and continuous improvement but also opens doors for new opportunities in partnerships, product launches and expansion into international markets. 
 
“This accomplishment affirms that our Quality Management System meets the rigorous standards required for the design, development and production of medical devices, and it positions us confidently for both regulatory and market success,” said Larisa Baesu, Senior Industry Adviser and Quality Manager at Endava. 

 

Our ISO 13485:2016 certification demonstrates our ability to deliver software for regulated medical devices and SaMD. Get in contact today if you would like to learn more.

 

About Endava:  

Endava is a leading provider of next-generation technology services, dedicated to enabling its customers to accelerate growth, tackle complex challenges and thrive in evolving markets. By combining innovative technologies and deep industry expertise with an AI-native approach, Endava consults and partners with customers to create solutions that drive transformation, augment intelligence and deliver lasting impact. From ideation to production, it supports customers with tailor-made solutions at every stage of their digital transformation, regardless of industry, region or scale.  

 

Endava’s clients span payments, insurance, finance and banking, technology, media, telecommunications, healthcare and life sciences, mobility, retail and consumer goods and more. As of December 31 2024, 11,668 Endavans are helping clients break new ground across locations in Europe, the Americas, Asia Pacific and the Middle East. 

 

 

 

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