Foshan RuiTong Consulting Co.,Ltd. (afterwards abbreviated as RuiTong) supports Anhui Xingzhou Pharma Co.,Ltd. (afterwards abbreviated as Xingzhou Pharma) to construct a full new pharmaceutical factory from a green space since June 16, 2021. Under the comprehensive guidance from RuiTong, RuiTong supports Xingzhou Pharma to design the workshop, warehouse and laboratory and supervise the quality of construction, and supports Xingzhou Pharma to establish the quality system, includes risk assessment, process modification, equipment qualification, documentation system, training, project management to ensure quality system of Xingzhou Pharma complies with requirements of Chinese GMP and US cGMP.

The APIs (Gluconolactone, Calcium Gluconate, Ferrous Gluconate, Zinc Gluconate) and quality system of Xingzhou Pharma was inspected by AH MPA inspector on June 01, 2023 and finally passed AH MPA on-site inspection with few deficiencies, Xingzhou Pharma obtained drug manufacturing license on August 07, 2023.

After obtaining drug manufacturing license, Xingzhou Pharma was changed from food enterprise to food and drug enterprise, which was the milestone affairs for Xingzhou Pharma, and which will vastly improve market competitiveness, we believe Xingzhou Pharma will be more prosperous and stronger. RuiTong will continue to lead Xingzhou Pharma to implement analytical methods validation, process validation, cleaning validation, quality study, Chinese and US DMF registration and ensure APIs of Xingzhou Pharma could enter domestic and aboard makets.

RuiTong throughout insists vision with “Customer Focus, Result oriented” and help customer do every detail well really. If you need to know more about our services related to GMP and drug registration (CEP/DMF/ASMF/PQ), please do not hesitate to contact us.

Foshan RuiTong Consulting Co.,Ltd.

Room 803, Fuwei Building, Huangqi, GuangFo Road No.1, Nanhai District, Foshan City, Guangdong Province, China

Website: http://www.gdruitong.cn/

Tel.: +86-13660057841, +86-13695153512