Enhance regulatory compliance and operational efficiency with our Medical Devices QMS Software (eQMS). Our solution streamlines document control, risk management, CAPA, audits, and regulatory compliance, ensuring adherence to ISO 13485, FDA 21 CFR Part 820, and MDR. Designed for medical device manufacturers, our eQMS optimizes quality processes, reducing errors and improving productivity. Operon Strategist provides expert guidance for seamless implementation, helping you maintain a compliant and efficient QMS. Get in touch today to upgrade your quality management system with our advanced eQMS solution.