01 1QUALIX DOT S.L. L’Hospitalet de Llobregat ES
01 1Etidronate disodium
01 1Blank
01 1Valid
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Certificate Number : CEP 2023-321 - Rev 00
Status : Valid
Issue Date : 2025-01-31
Type : Chemical
Substance Number : 1778
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PharmaCompass offers a list of Etidronate Disodium 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 Etidronate Disodium manufacturer or Etidronate Disodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etidronate Disodium manufacturer or Etidronate Disodium supplier.
PharmaCompass also assists you with knowing the Etidronate Disodium API Price utilized in the formulation of products. Etidronate Disodium API Price is not always fixed or binding as the Etidronate Disodium Price is obtained through a variety of data sources. The Etidronate Disodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etidronate Disodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etidronate Disodium, including repackagers and relabelers. The FDA regulates Etidronate Disodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etidronate Disodium 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 Etidronate Disodium supplier is an individual or a company that provides Etidronate Disodium active pharmaceutical ingredient (API) or Etidronate Disodium finished formulations upon request. The Etidronate Disodium suppliers may include Etidronate Disodium API manufacturers, exporters, distributors and traders.
click here to find a list of Etidronate Disodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etidronate Disodium CEP of the European Pharmacopoeia monograph is often referred to as a Etidronate Disodium Certificate of Suitability (COS). The purpose of a Etidronate Disodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etidronate Disodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etidronate Disodium to their clients by showing that a Etidronate Disodium CEP has been issued for it. The manufacturer submits a Etidronate Disodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etidronate Disodium CEP holder for the record. Additionally, the data presented in the Etidronate Disodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etidronate Disodium DMF.
A Etidronate Disodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etidronate Disodium 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 Etidronate Disodium suppliers with CEP (COS) on PharmaCompass.
