01 2KYOWA HAKKO BIO CO., LTD. Tokyo JP
01 2Glutathione
01 2Japan
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2020-328 - Rev 00
Status : Valid
Issue Date : 2023-01-13
Type : Chemical
Substance Number : 1670
Certificate Number : R0-CEP 2014-174 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2016-06-09
Type : Chemical
Substance Number : 1670
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PharmaCompass offers a list of Glutathione API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Glutathione manufacturer or Glutathione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glutathione manufacturer or Glutathione supplier.
PharmaCompass also assists you with knowing the Glutathione API Price utilized in the formulation of products. Glutathione API Price is not always fixed or binding as the Glutathione Price is obtained through a variety of data sources. The Glutathione Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tathione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tathione, including repackagers and relabelers. The FDA regulates Tathione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tathione 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 Tathione manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tathione supplier is an individual or a company that provides Tathione active pharmaceutical ingredient (API) or Tathione finished formulations upon request. The Tathione suppliers may include Tathione API manufacturers, exporters, distributors and traders.
click here to find a list of Tathione suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tathione CEP of the European Pharmacopoeia monograph is often referred to as a Tathione Certificate of Suitability (COS). The purpose of a Tathione CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tathione EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tathione to their clients by showing that a Tathione CEP has been issued for it. The manufacturer submits a Tathione CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tathione CEP holder for the record. Additionally, the data presented in the Tathione CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tathione DMF.
A Tathione CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tathione CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Tathione suppliers with CEP (COS) on PharmaCompass.
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