Policies, strategies, and action plans for health technologies, specifically for medical devices, are required in any national health plan. Within the context of a robust health system they ensure access to safe, effective, and high-quality medical devices that prevent, diagnose, and treat disease and injury, and assist patients in their rehabilitation.
Our quality management team provides customers with products that strictly comply with WHO’s “Demonstration of Global Regulatory Framework for Medical Devices, including in vitro Diagnostic medical Devices,” as well as meeting the specific requirements of customers’ domestic markets. Additionally, we offer support to our customers in registering Sinophare products in their respective destination countries.
