Degas Company strictly abides by GMP standards, owns good production equipment, reasonable production processes, perfect quality management and strict inspection systems to ensure the quality of the final product and meets the legal requirements.
And strictly follow the three elements of GMP. The first is to minimize human errors; the second is to prevent the pollution of pharmaceuticals and the production of low-quality pharmaceuticals; and the third is to ensure the high-quality system design of the product.
The full name of ISO13485 is "Medical Devices-Quality Management System-Requirements for Regulations". This standard was formulated by the ISO/TC 210-Medical Device Quality Management and General Requirements Standardization Technical Committee, including design and development, sample manufacturing, registration testing, and clinical trials, product registration, product production, product sales, product use and other medical device production links.
Degas strictly follows the ISO13485 quality management system to ensure that Dearcare can provide medical device products that meet customer requirements and applicable regulatory requirements and provide consumers and professionals with confidence.
In order to ensure the safety and effectiveness of medical devices, and protect human health and life safety, Dearcare strictly abides by the requirements of the Guangdong Food and Drug Administration and follows the "Regulations on the Supervision and Administration of Medical Devices." Dearcare has strictly supervised the product quality during the operation of the company, and regularly inspected and assessed the implementation of the company's quality management work, also insisted on quality training and education for the internal personnel.