News Center


Taian Mainland Medical Devices Co., Ltd

2011


The company has a 100,000-level clean production workshop of more than 20,000 square meters, which is fully operated in accordance with GMP requirements, and is equipped with personnel and material purification facilities; the dust-producing room is designed with full exhaust air to avoid cross-contamination. The company has passed the ISO 13485 quality system certification, and strictly implements the relevant standard operating procedures and management procedures during the production process to ensure that each product meets the quality standards.

Previous Page

Next Page