01 1QUALITY CHEMICALS S.L. Esparreguera ES
01 1Disodium phosphate dodecahydrate
01 1Spain
01 1Valid
Disodium Phosphate Dodecahydrate
Certificate Number : CEP 2017-233 - Rev 02
Status : Valid
Issue Date : 2023-10-23
Type : Chemical
Substance Number : 118
46
PharmaCompass offers a list of Disodium Hydrogen Phosphate 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 Disodium Hydrogen Phosphate manufacturer or Disodium Hydrogen Phosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Disodium Hydrogen Phosphate API Price utilized in the formulation of products. Disodium Hydrogen Phosphate API Price is not always fixed or binding as the Disodium Hydrogen Phosphate Price is obtained through a variety of data sources. The Disodium Hydrogen Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate, including repackagers and relabelers. The FDA regulates Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate 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 Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate supplier is an individual or a company that provides Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate active pharmaceutical ingredient (API) or Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate finished formulations upon request. The Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate suppliers may include Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate API manufacturers, exporters, distributors and traders.
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A Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP of the European Pharmacopoeia monograph is often referred to as a Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate Certificate of Suitability (COS). The purpose of a Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate to their clients by showing that a Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP has been issued for it. The manufacturer submits a Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP holder for the record. Additionally, the data presented in the Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate DMF.
A Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Buffer solution from phosphoric acid/di-Sodium hydrogen phosphate 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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