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01 1Nippon Protein Co., Ltd. Ashikaga-shi JP
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01 1Cysteine Hydrochloride Monohydrate
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01 1Japan
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01 1Valid
Cysteine Hydrochloride Monohydrate
Certificate Number : R1-CEP 2003-159 - Rev 03
Status : Valid
Issue Date : 2014-08-05
Type : Chemical
Substance Number : 895
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PharmaCompass offers a list of L-Cysteine 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 L-Cysteine manufacturer or L-Cysteine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Cysteine manufacturer or L-Cysteine supplier.
PharmaCompass also assists you with knowing the L-Cysteine API Price utilized in the formulation of products. L-Cysteine API Price is not always fixed or binding as the L-Cysteine Price is obtained through a variety of data sources. The L-Cysteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cys manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cys, including repackagers and relabelers. The FDA regulates Cys manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cys 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 Cys manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cys supplier is an individual or a company that provides Cys active pharmaceutical ingredient (API) or Cys finished formulations upon request. The Cys suppliers may include Cys API manufacturers, exporters, distributors and traders.
click here to find a list of Cys suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cys CEP of the European Pharmacopoeia monograph is often referred to as a Cys Certificate of Suitability (COS). The purpose of a Cys CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cys EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cys to their clients by showing that a Cys CEP has been issued for it. The manufacturer submits a Cys CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cys CEP holder for the record. Additionally, the data presented in the Cys CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cys DMF.
A Cys CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cys 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 Cys suppliers with CEP (COS) on PharmaCompass.
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