01 1BORAX FRANCAIS Coudekerque-Branche FR
01 1Borax, Granular and powder
01 1U.S.A
01 1Valid
Certificate Number : R1-CEP 2009-207 - Rev 05
Status : Valid
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 13
25
PharmaCompass offers a list of Borax Solution 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 Borax Solution manufacturer or Borax Solution supplier for your needs.
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PharmaCompass also assists you with knowing the Borax Solution API Price utilized in the formulation of products. Borax Solution API Price is not always fixed or binding as the Borax Solution Price is obtained through a variety of data sources. The Borax Solution Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium tetraborate buffer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium tetraborate buffer, including repackagers and relabelers. The FDA regulates Sodium tetraborate buffer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium tetraborate buffer API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Sodium tetraborate buffer supplier is an individual or a company that provides Sodium tetraborate buffer active pharmaceutical ingredient (API) or Sodium tetraborate buffer finished formulations upon request. The Sodium tetraborate buffer suppliers may include Sodium tetraborate buffer API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium tetraborate buffer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium tetraborate buffer CEP of the European Pharmacopoeia monograph is often referred to as a Sodium tetraborate buffer Certificate of Suitability (COS). The purpose of a Sodium tetraborate buffer CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sodium tetraborate buffer EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sodium tetraborate buffer to their clients by showing that a Sodium tetraborate buffer CEP has been issued for it. The manufacturer submits a Sodium tetraborate buffer CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sodium tetraborate buffer CEP holder for the record. Additionally, the data presented in the Sodium tetraborate buffer CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sodium tetraborate buffer DMF.
A Sodium tetraborate buffer CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sodium tetraborate buffer 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 tetraborate buffer suppliers with CEP (COS) on PharmaCompass.
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