01 1ESTEVE QUIMICA S.A. Barcelona ES
02 1FSP GALENA Wroclaw PL
01 1Etamsylate
02 1Etamsylate, Code 0122-P54 - Code 0122-P57
01 1Poland
02 1Spain
01 2Valid
Etamsylate, Code 0122-P54 - Code 0122-P57
Certificate Number : R1-CEP 1997-070 - Rev 08
Status : Valid
Issue Date : 2019-11-22
Type : Chemical
Substance Number : 1204
Certificate Number : R1-CEP 2008-317 - Rev 04
Status : Valid
Issue Date : 2022-10-28
Type : Chemical
Substance Number : 1204
95
PharmaCompass offers a list of Ethamsylate 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 Ethamsylate manufacturer or Ethamsylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethamsylate manufacturer or Ethamsylate supplier.
PharmaCompass also assists you with knowing the Ethamsylate API Price utilized in the formulation of products. Ethamsylate API Price is not always fixed or binding as the Ethamsylate Price is obtained through a variety of data sources. The Ethamsylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etamsilato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etamsilato, including repackagers and relabelers. The FDA regulates Etamsilato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etamsilato 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 Etamsilato manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etamsilato supplier is an individual or a company that provides Etamsilato active pharmaceutical ingredient (API) or Etamsilato finished formulations upon request. The Etamsilato suppliers may include Etamsilato API manufacturers, exporters, distributors and traders.
click here to find a list of Etamsilato suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etamsilato CEP of the European Pharmacopoeia monograph is often referred to as a Etamsilato Certificate of Suitability (COS). The purpose of a Etamsilato CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etamsilato EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etamsilato to their clients by showing that a Etamsilato CEP has been issued for it. The manufacturer submits a Etamsilato CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etamsilato CEP holder for the record. Additionally, the data presented in the Etamsilato CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etamsilato DMF.
A Etamsilato CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etamsilato 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 Etamsilato suppliers with CEP (COS) on PharmaCompass.
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