01 1Shandong Jin cheng Bio-Pharmaceutical Co., Ltd.
02 1Shandong Jincheng Bio-pharmaceutical Co., Ltd
01 1Hiple Co., Ltd.
02 1SG Biochem Co., Ltd.
01 2Glutathione (reduced)
01 2China
Registrant Name : SG Biochem Co., Ltd.
Registration Date : 2021-08-27
Registration Number : 20200629-211-J-663(1)
Manufacturer Name : Shandong Jincheng Bio-pharma...
Manufacturer Address : Jiao Wang Fu Xian Road North, Dong Yi Road West, Zichuan Economy Development Zone, Zi...
Registrant Name : Hiple Co., Ltd.
Registration Date : 2020-06-29
Registration Number : 20200629-211-J-663
Manufacturer Name : Shandong Jin cheng Bio-Pharm...
Manufacturer Address : Jiao Wang Fu Xian Road North, Dong Yi Road West, Zichuan Economy Development Zone, Zi...
A Glutathione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glutathione, including repackagers and relabelers. The FDA regulates Glutathione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glutathione API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Glutathione manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glutathione supplier is an individual or a company that provides Glutathione active pharmaceutical ingredient (API) or Glutathione finished formulations upon request. The Glutathione suppliers may include Glutathione API manufacturers, exporters, distributors and traders.
click here to find a list of Glutathione suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Glutathione Drug Master File in Korea (Glutathione KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Glutathione. The MFDS reviews the Glutathione KDMF as part of the drug registration process and uses the information provided in the Glutathione KDMF to evaluate the safety and efficacy of the drug.
After submitting a Glutathione KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Glutathione API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Glutathione suppliers with KDMF on PharmaCompass.
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