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.
AQAP (Allied Quality Assurance Publications) is a NATO-originated guideline for quality management in defense-related projects. Specifically, AQAP-2110 sets rigorous requirements for processes, documentation, and configuration management in defense and aerospace programs. Certification is the most recognized way to demonstrate compliance with these standards.
9001 is a globally respected quality management standard that ensures that organizations follow structured, consistent processes to deliver products and services that meet customer and regulatory expectations. For AQAP certification, ISO 9001 is a prerequisite for most certification companies.
