1. The company has passed ISO9001-2016 quality system certification. With reference to ICH Q7 and GMP requirements, the company continues to upgrade the quality system and plans to establish a quality management system that meets the production of pharmaceutical intermediates.

2, The analysis center matching the production capacity is equipped with 5 Agilent liquid chromatograph (HPLC), 4 Agilent gas Chromatograph (GC), METTler moisture detector, METTler analysis electronic balance (1/10,000) and other equipment to meet the production quality delivery.

3, Quality audit: Since 2019 has accepted customer quality audit 6 times

2022.07 Passed the quality audit of Chongqing Porton Pharmaceutical Technology Co., LTD.
2022.07 / Chongqing Porton  in China/ Quality audit

2022.06 Passed the quality audit of Zhejiang Huahai Pharmaceutical Co., LTD.
2022.06 / Zhejiang Huahai Pharmaceutical Corporation in China/ Quality audit

2022.05 Passed quality audit of AMI in India
2022.05 / AMI in India/ Quality audit

2022.02 Passed quality audit by Aurobindo India
2022.02 / Aurobindo in India/ Quality audit

2021.09 Passed the quality audit of Jiangxi Porton Pharmaceutical
2021.09 / Jiangxi Port & NBSP; in China/ Quality audit

2020.07 Passed the quality audit of Mitsu Co., LTD
2020.07 / Mitsuko Corporation in Japan/ Quality audit