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