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