At Evnia, we enable manufacturers of medical devices, in-vitro diagnostic medical devices and pharmaceuticals worldwide to achieve and remain in compliance with global regulatory requirements and to ensure audit and inspection readiness.
Our full-value-chain services are supported by a growing, cross-functional team of medical writers, medical doctors, engineers for usability, risk and validation, biostatisticians, biocompatibility experts and regulatory affair executives. Our in-house human resources enable the development and implementation of holistic approaches covering the entire lifetime of medical devices, IVDs or pharmaceuticals.