To meet customer requirements on products, we practice customer-centric management while introducing and implementing communication processes and other customer service processes in accordance with GMP standards.
- GMP certificate for in-vitro medical devices manufacturing and quality management, Ministry of Food and Drug Safety GMP certificate for in-vitro medical devices manufacturing and quality management, Ministry of Food and Drug Safety
- ISO 13485 for Medical devices – Quality management systems – Requirements for regulatory purposes, BSI (British Standards)
- GMP certificate for medical devices, Ministry of Food and Drug Safety
- Corporate Affiliated Research Institute Certificate (Seegene Inc. R&D Life Sciences)