Case Study: ViViRA accelerates MDR approval and documentation with Matrix Requirements

ViViRA brings digital alternative to physiotherapy to back pain patients across Germany

ViViRA, a startup providing a digital physiotherapy app, needed to effectively manage its journey to MDR regulatory approval for its Class IIa medical device. Their previous tools were inefficient and not designed for medical devices, risking delays. To maintain startup agility and ensure compliance, they sought a faster approach to quality and application lifecycle management and chose the MatrixReq solution from Matrix Requirements.

By implementing MatrixReq, ViViRA gained an automated, end-to-end platform for managing requirements, risks, tests, and documentation. This solution from Matrix Requirements enabled a 50% faster review and approval process and slashed documentation generation time by 97%, from 8 hours to just 15 minutes. The migration was completed in two weeks, accelerating their path to MDR approval and ensuring long-term agility for future app releases.

ViViRA

Sven Büttner

Head of Quality and Regulatory