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
22
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Borax Solution manufacturer or Borax Solution supplier.
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 borate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of sodium borate, including repackagers and relabelers. The FDA regulates sodium borate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. sodium borate 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 borate supplier is an individual or a company that provides sodium borate active pharmaceutical ingredient (API) or sodium borate finished formulations upon request. The sodium borate suppliers may include sodium borate API manufacturers, exporters, distributors and traders.
click here to find a list of sodium borate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A sodium borate CEP of the European Pharmacopoeia monograph is often referred to as a sodium borate Certificate of Suitability (COS). The purpose of a sodium borate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of sodium borate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of sodium borate to their clients by showing that a sodium borate CEP has been issued for it. The manufacturer submits a sodium borate CEP (COS) as part of the market authorization procedure, and it takes on the role of a sodium borate CEP holder for the record. Additionally, the data presented in the sodium borate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the sodium borate DMF.
A sodium borate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. sodium borate 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 borate suppliers with CEP (COS) on PharmaCompass.
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