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01 1LA MESTA CHIMIE FINE Gilette FR
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01 1Hexamidine diisetionate
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01 1France
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01 1Valid
Certificate Number : R1-CEP 1999-106 - Rev 05
Status : Valid
Issue Date : 2017-12-06
Type : Chemical
Substance Number : 1436
17
PharmaCompass offers a list of Hexamidine 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 Hexamidine manufacturer or Hexamidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexamidine manufacturer or Hexamidine supplier.
PharmaCompass also assists you with knowing the Hexamidine API Price utilized in the formulation of products. Hexamidine API Price is not always fixed or binding as the Hexamidine Price is obtained through a variety of data sources. The Hexamidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hexamidin 2-hydroxyethansulfonat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexamidin 2-hydroxyethansulfonat, including repackagers and relabelers. The FDA regulates Hexamidin 2-hydroxyethansulfonat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexamidin 2-hydroxyethansulfonat 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 Hexamidin 2-hydroxyethansulfonat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexamidin 2-hydroxyethansulfonat supplier is an individual or a company that provides Hexamidin 2-hydroxyethansulfonat active pharmaceutical ingredient (API) or Hexamidin 2-hydroxyethansulfonat finished formulations upon request. The Hexamidin 2-hydroxyethansulfonat suppliers may include Hexamidin 2-hydroxyethansulfonat API manufacturers, exporters, distributors and traders.
click here to find a list of Hexamidin 2-hydroxyethansulfonat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexamidin 2-hydroxyethansulfonat CEP of the European Pharmacopoeia monograph is often referred to as a Hexamidin 2-hydroxyethansulfonat Certificate of Suitability (COS). The purpose of a Hexamidin 2-hydroxyethansulfonat CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hexamidin 2-hydroxyethansulfonat EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hexamidin 2-hydroxyethansulfonat to their clients by showing that a Hexamidin 2-hydroxyethansulfonat CEP has been issued for it. The manufacturer submits a Hexamidin 2-hydroxyethansulfonat CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hexamidin 2-hydroxyethansulfonat CEP holder for the record. Additionally, the data presented in the Hexamidin 2-hydroxyethansulfonat CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hexamidin 2-hydroxyethansulfonat DMF.
A Hexamidin 2-hydroxyethansulfonat CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hexamidin 2-hydroxyethansulfonat 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 Hexamidin 2-hydroxyethansulfonat suppliers with CEP (COS) on PharmaCompass.
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