01 1DR. PAUL LOHMANN GMBH & CO. KGAA Emmerthal DE
02 1QUALITY CHEMICALS S.L. Esparreguera ES
01 2Sodium dihydrogen phosphate dihydrate
01 1Germany
02 1Spain
01 2Valid
Sodium Dihydrogen Phosphate Dihydrate
Certificate Number : CEP 2019-228 - Rev 01
Status : Valid
Issue Date : 2023-10-04
Type : Chemical
Substance Number : 194
Sodium Dihydrogen Phosphate Dihydrate
Certificate Number : CEP 2017-177 - Rev 02
Status : Valid
Issue Date : 2023-09-26
Type : Chemical
Substance Number : 194
A Sodium Dihydrogen Phosphate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Dihydrogen Phosphate Dihydrate, including repackagers and relabelers. The FDA regulates Sodium Dihydrogen Phosphate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Dihydrogen Phosphate Dihydrate 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 Sodium Dihydrogen Phosphate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Dihydrogen Phosphate Dihydrate supplier is an individual or a company that provides Sodium Dihydrogen Phosphate Dihydrate active pharmaceutical ingredient (API) or Sodium Dihydrogen Phosphate Dihydrate finished formulations upon request. The Sodium Dihydrogen Phosphate Dihydrate suppliers may include Sodium Dihydrogen Phosphate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Dihydrogen Phosphate Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Dihydrogen Phosphate Dihydrate CEP of the European Pharmacopoeia monograph is often referred to as a Sodium Dihydrogen Phosphate Dihydrate Certificate of Suitability (COS). The purpose of a Sodium Dihydrogen Phosphate Dihydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium Dihydrogen Phosphate Dihydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium Dihydrogen Phosphate Dihydrate to their clients by showing that a Sodium Dihydrogen Phosphate Dihydrate CEP has been issued for it. The manufacturer submits a Sodium Dihydrogen Phosphate Dihydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium Dihydrogen Phosphate Dihydrate CEP holder for the record. Additionally, the data presented in the Sodium Dihydrogen Phosphate Dihydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium Dihydrogen Phosphate Dihydrate DMF.
A Sodium Dihydrogen Phosphate Dihydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium Dihydrogen Phosphate Dihydrate 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 Sodium Dihydrogen Phosphate Dihydrate suppliers with CEP (COS) on PharmaCompass.
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