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 059QF0KO0R manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 059QF0KO0R, including repackagers and relabelers. The FDA regulates 059QF0KO0R manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 059QF0KO0R 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 059QF0KO0R supplier is an individual or a company that provides 059QF0KO0R active pharmaceutical ingredient (API) or 059QF0KO0R finished formulations upon request. The 059QF0KO0R suppliers may include 059QF0KO0R API manufacturers, exporters, distributors and traders.
click here to find a list of 059QF0KO0R suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 059QF0KO0R CEP of the European Pharmacopoeia monograph is often referred to as a 059QF0KO0R Certificate of Suitability (COS). The purpose of a 059QF0KO0R CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 059QF0KO0R EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 059QF0KO0R to their clients by showing that a 059QF0KO0R CEP has been issued for it. The manufacturer submits a 059QF0KO0R CEP (COS) as part of the market authorization procedure, and it takes on the role of a 059QF0KO0R CEP holder for the record. Additionally, the data presented in the 059QF0KO0R CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 059QF0KO0R DMF.
A 059QF0KO0R CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 059QF0KO0R 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 059QF0KO0R suppliers with CEP (COS) on PharmaCompass.
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