01 1Gaylord Chemical Company L.L.C Slidell US
02 1TORAY FINE CHEMICALS CO., LTD Chiyoda-ku JP
01 2Dimethyl sulfoxide
01 1India
02 1U.S.A
01 2Valid
Certificate Number : R1-CEP 2012-365 - Rev 00
Status : Valid
Issue Date : 2019-02-25
Type : Chemical
Substance Number : 763
Certificate Number : CEP 2023-062 - Rev 00
Status : Valid
Issue Date : 2024-08-06
Type : Chemical
Substance Number : 763
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PharmaCompass offers a list of Dimethyl Sulfoxide 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 Dimethyl Sulfoxide manufacturer or Dimethyl Sulfoxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimethyl Sulfoxide manufacturer or Dimethyl Sulfoxide supplier.
PharmaCompass also assists you with knowing the Dimethyl Sulfoxide API Price utilized in the formulation of products. Dimethyl Sulfoxide API Price is not always fixed or binding as the Dimethyl Sulfoxide Price is obtained through a variety of data sources. The Dimethyl Sulfoxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Decap manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Decap, including repackagers and relabelers. The FDA regulates Decap manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Decap API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Decap supplier is an individual or a company that provides Decap active pharmaceutical ingredient (API) or Decap finished formulations upon request. The Decap suppliers may include Decap API manufacturers, exporters, distributors and traders.
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A Decap CEP of the European Pharmacopoeia monograph is often referred to as a Decap Certificate of Suitability (COS). The purpose of a Decap CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Decap EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Decap to their clients by showing that a Decap CEP has been issued for it. The manufacturer submits a Decap CEP (COS) as part of the market authorization procedure, and it takes on the role of a Decap CEP holder for the record. Additionally, the data presented in the Decap CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Decap DMF.
A Decap CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Decap CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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