Hubei Gedian Humanwell pharmaceutical Co., Ltd. was founded in 2000 and started API production in 2003
2004
Gedian Humanwell were approved by C-FDA and certified with GMP certification
2006
Cyproterone Acetate was certified with CEP
2009
Our Formulation Plant, Jiulong Humanwell Pharmaceutical Co., Ltd. was founded, production started in 2012
2011
Our raw material plant, Hubei Zhuxi Humanwell Pharmaceutical Co., Ltd. was founded, production started in 2013
2012
Wuhan Jiulong Pharmaceutical Co., Ltd. , the trade platform was founded
Hubei Gedian Humanwell Pharmaceutical Excipients Co., Ltd. was founded
2013
Gedian Humanwell were approved by US FDA for Progesterone and Finasteride
2016
Gedian Humanwell were approved by EDQM for Progesterone, and certified with EU GMP
2019
Gedian Humanwell were approved by Japan PMDA for Finasteride
2020
We were approved by Australian TGA for Cyproterone Acetate
2021
A new modern API factory - Huanggang Humanwell Pharmaceutical Co., Ltd. was founded
2023
Gedian Humanwell were approved by MFDS for Oxcarbazepine and Dutasteride
2024
Gedian Humanwell were approved by EDQM for Cyproterone Acetate
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