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Tonggak Utama

2000

Hubei Gedian Humanwell pharmaceutical Co., Ltd. didegaké ing 2000 lan miwiti produksi API ing 2003

2004

Gedian Humanwell disetujoni dening C-FDA lan disertifikasi karo sertifikasi GMP

2006

Cyproterone Acetate disertifikasi karo CEP

2009

Pabrik Formulasi kita, Jiulong Humanwell Pharmaceutical Co., Ltd. didegake, produksi diwiwiti ing 2012

2011

Pabrik bahan mentah kita, Hubei Zhuxi Humanwell Pharmaceutical Co., Ltd. didegake, produksi diwiwiti ing 2013

2012

Wuhan Jiulong Pharmaceutical Co., Ltd., platform perdagangan didegaké
Hubei Gedian Humanwell Pharmaceutical Excipients Co., Ltd. didegake

2013

Gedian Humanwell disetujoni dening US FDA kanggo Progesteron lan Finasteride

2016

Gedian Humanwell disetujoni dening EDQM kanggo Progesteron, lan disertifikasi karo GMP EU

2019

Gedian Humanwell disetujoni dening PMDA Jepang kanggo Finasteride

2020

Kita disetujoni dening TGA Australia kanggo Cyproterone Acetate

2021

Pabrik API modern anyar - Huanggang Humanwell Pharmaceutical Co., Ltd. didegake

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