Innokas utilizes ISO 13485 as a standard of its operations. Generally, ISO 13485 is a standard for managing the quality of medical devices and applies to organizations engaged in designing, producing, and servicing medical devices. Innokas applies ISO 13485 on a more diverse level as a proof of capability to working with any sort of complicated solution concept. ISO 13485 certified company is committed to regulatory compliance, ongoing risk management across the device's lifecycle, and a focus on documentation, traceability, and quality control on any device.
While our core certificate ISO 13485 is widely recognized as a medical certificate, its principles of quality management and strict standards can be adapted to various industries. See how this versatile framework can elevate excellence across diverse sectors.
