On December 20, 2019, Shandong Jiulong Hisince Pharmaceutical Co., Ltd. was audited by the Shandong GMP expert team and passed the GMP retest.

 

After listening to the company's various work reports, the expert group, accompanied by the general manager and the manager of the quality assurance department, conducted strict, detailed and comprehensive inspections of the company's laboratories, clean zones, production workshops, warehouses, etc. The acceptance team also carefully reviewed and inspected the employee files, batch production records, and finished product sales records. After a comprehensive inspection of Shandong Jiulong Hengxin Pharmaceutical, the expert group gave a high degree of affirmation to the company's various work. They agreed that Shandong Jiulong Hengxin Pharmaceutical had a sound organizational structure and clear functions; the plant layout was reasonable and environmental sanitation met the requirements; production, The inspection equipment and management documents are complete, and all inspections meet the requirements. Shandong Jiulong Hengxin Pharmaceutical Co., Ltd. successfully passed the re-inspection with excellent results.

 

Since 2015, this re-inspection is the third time that Shandong Jiulong Hengxin Pharmaceutical has successfully passed the GMP inspection, marking that our company's production and quality management level has reached a new level, and it has also laid a foundation for further improving the company's industry competitiveness A solid foundation.