Evnia introduces a paradigm shift in the MedTech consulting services by offering expert medical device lifecycle management services.
We support manufacturers throughout the medical device development roadmap. From the early concept and design stages to verification and validation, until market access and post-market adulthood, Evnia enables compliances and ensures audit and inspection readiness.
Within this context, we help manufacturers and inventors globally to develop comprehensive post-market surveillance strategies that reflect the data collection needs of their portfolio. PMS is the tool for understanding device performance and improving quality and R&D.
Find out more about Evnia’s Vigilance Algorithm EVA here!
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