We are proud to have received several domestic and international product and system certificates
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
ISO 13485 is an internationally recognized standard set of requirements issued by the International Organization for Standardization (ISO) to create a Quality Management System for those in the medical device industry.
ISO 15378 specifies quality management system requirements for primary packaging manufacturers in the pharmaceutical and medical device industries