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01 1BORAX FRANCAIS Coudekerque-Branche FR
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01 1Borax, Granular and powder
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01 1U.S.A
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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.
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 Komex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Komex, including repackagers and relabelers. The FDA regulates Komex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Komex 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 Komex supplier is an individual or a company that provides Komex active pharmaceutical ingredient (API) or Komex finished formulations upon request. The Komex suppliers may include Komex API manufacturers, exporters, distributors and traders.
click here to find a list of Komex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Komex CEP of the European Pharmacopoeia monograph is often referred to as a Komex Certificate of Suitability (COS). The purpose of a Komex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Komex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Komex to their clients by showing that a Komex CEP has been issued for it. The manufacturer submits a Komex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Komex CEP holder for the record. Additionally, the data presented in the Komex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Komex DMF.
A Komex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Komex 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 Komex suppliers with CEP (COS) on PharmaCompass.