01 1Uniqema Gouda NL
01 1Fatty acid sodium soap base, Prisavon® 1983, Prisavon® 9249, Prisavon® 9250, Prisavon® 9251, Prisavon® 9253,
01 1Spain
01 1Expired
Fatty Acid Sodium Soap Base, Prisavon® 1983, Pr...
Certificate Number : R0-CEP 2001-100 - Rev 01
Status : Expired
Issue Date : 2005-03-22
Type : TSE
Substance Number :
28
PharmaCompass offers a list of Sodium Butyrate 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 Sodium Butyrate manufacturer or Sodium Butyrate supplier for your needs.
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A Kyselina maselna [Czech] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kyselina maselna [Czech], including repackagers and relabelers. The FDA regulates Kyselina maselna [Czech] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kyselina maselna [Czech] 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 Kyselina maselna [Czech] supplier is an individual or a company that provides Kyselina maselna [Czech] active pharmaceutical ingredient (API) or Kyselina maselna [Czech] finished formulations upon request. The Kyselina maselna [Czech] suppliers may include Kyselina maselna [Czech] API manufacturers, exporters, distributors and traders.
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A Kyselina maselna [Czech] CEP of the European Pharmacopoeia monograph is often referred to as a Kyselina maselna [Czech] Certificate of Suitability (COS). The purpose of a Kyselina maselna [Czech] CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Kyselina maselna [Czech] EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Kyselina maselna [Czech] to their clients by showing that a Kyselina maselna [Czech] CEP has been issued for it. The manufacturer submits a Kyselina maselna [Czech] CEP (COS) as part of the market authorization procedure, and it takes on the role of a Kyselina maselna [Czech] CEP holder for the record. Additionally, the data presented in the Kyselina maselna [Czech] CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Kyselina maselna [Czech] DMF.
A Kyselina maselna [Czech] CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Kyselina maselna [Czech] 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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