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
91
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 Aqua Purificata manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aqua Purificata, including repackagers and relabelers. The FDA regulates Aqua Purificata manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aqua Purificata 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 Aqua Purificata manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aqua Purificata supplier is an individual or a company that provides Aqua Purificata active pharmaceutical ingredient (API) or Aqua Purificata finished formulations upon request. The Aqua Purificata suppliers may include Aqua Purificata API manufacturers, exporters, distributors and traders.
click here to find a list of Aqua Purificata suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aqua Purificata CEP of the European Pharmacopoeia monograph is often referred to as a Aqua Purificata Certificate of Suitability (COS). The purpose of a Aqua Purificata CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aqua Purificata EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aqua Purificata to their clients by showing that a Aqua Purificata CEP has been issued for it. The manufacturer submits a Aqua Purificata CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aqua Purificata CEP holder for the record. Additionally, the data presented in the Aqua Purificata CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aqua Purificata DMF.
A Aqua Purificata CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aqua Purificata 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 Aqua Purificata suppliers with CEP (COS) on PharmaCompass.
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