01 1CSL BEHRING GMBH Marburg DE
01 1Water for injections, Sterilised
01 1U.S.A
01 1Valid
Water For Injections, Sterilised
Certificate Number : CEP 2024-246 - Rev 00
Status : Valid
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 169
23
PharmaCompass offers a list of Water 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 Water manufacturer or Water supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Water manufacturer or Water supplier.
PharmaCompass also assists you with knowing the Water API Price utilized in the formulation of products. Water API Price is not always fixed or binding as the Water Price is obtained through a variety of data sources. The Water Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dihydrogen oxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dihydrogen oxide, including repackagers and relabelers. The FDA regulates Dihydrogen oxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dihydrogen oxide 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 Dihydrogen oxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dihydrogen oxide supplier is an individual or a company that provides Dihydrogen oxide active pharmaceutical ingredient (API) or Dihydrogen oxide finished formulations upon request. The Dihydrogen oxide suppliers may include Dihydrogen oxide API manufacturers, exporters, distributors and traders.
click here to find a list of Dihydrogen oxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dihydrogen oxide CEP of the European Pharmacopoeia monograph is often referred to as a Dihydrogen oxide Certificate of Suitability (COS). The purpose of a Dihydrogen oxide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dihydrogen oxide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dihydrogen oxide to their clients by showing that a Dihydrogen oxide CEP has been issued for it. The manufacturer submits a Dihydrogen oxide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dihydrogen oxide CEP holder for the record. Additionally, the data presented in the Dihydrogen oxide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dihydrogen oxide DMF.
A Dihydrogen oxide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dihydrogen oxide 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 Dihydrogen oxide suppliers with CEP (COS) on PharmaCompass.
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