On January 14, 2014, under GMP requirements (2010), VP Li Mingkun and Quality Manager He Yuankai carried out site audit at coating material supplier Yingmao Pharmaceutical Co., Ltd in Beijing.
        The auditors carried out strict and meticulous audit of Yingmao's quality management system, production operation management system, material management and equipment management, and concluded that the company had perfect manpower & organizational structure and complete licenses & documents, meeting the specified requirements; layout of the production premises was reasonably arranged, the production & testing equipment was complete, well enough to meet the need of production and testing; the main equipment is verified; the production management is sound; the material & product management is virtually normalized; the production & quality management documents are complete. At last, the enterprise was found compliant with the requirements of Drug Production GMP (2010 Revision).