QAdvis is one of Europe’s leading specialized quality and regulatory consultant firms within medical devices and in-vitro diagnostic devices. We offer a complete range of services such as; regulatory affairs, quality management systems, risk management, software process, clinical evaluations, audits, training, interim management. We are active participants in several key international standardization committees and EU Commission workgroups, writing standards and guidelines. Let us help you with a solid and cost-effective approach to your regulatory challenges.