01 1SRI KRISHNA PHARMACEUTICALS LIMITED Hyderabad IN
01 1Sodium phenylbutyrate
01 1India
01 1Valid
Certificate Number : R0-CEP 2020-082 - Rev 00
Status : Valid
Issue Date : 2023-05-09
Type : Chemical
Substance Number : 2183
84
PharmaCompass offers a list of Sodium Phenylbutyrate 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 Phenylbutyrate manufacturer or Sodium Phenylbutyrate supplier for your needs.
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A S4125,1716-12-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S4125,1716-12-7, including repackagers and relabelers. The FDA regulates S4125,1716-12-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S4125,1716-12-7 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 S4125,1716-12-7 supplier is an individual or a company that provides S4125,1716-12-7 active pharmaceutical ingredient (API) or S4125,1716-12-7 finished formulations upon request. The S4125,1716-12-7 suppliers may include S4125,1716-12-7 API manufacturers, exporters, distributors and traders.
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A S4125,1716-12-7 CEP of the European Pharmacopoeia monograph is often referred to as a S4125,1716-12-7 Certificate of Suitability (COS). The purpose of a S4125,1716-12-7 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of S4125,1716-12-7 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of S4125,1716-12-7 to their clients by showing that a S4125,1716-12-7 CEP has been issued for it. The manufacturer submits a S4125,1716-12-7 CEP (COS) as part of the market authorization procedure, and it takes on the role of a S4125,1716-12-7 CEP holder for the record. Additionally, the data presented in the S4125,1716-12-7 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the S4125,1716-12-7 DMF.
A S4125,1716-12-7 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. S4125,1716-12-7 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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