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.
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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 00612_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 00612_FLUKA, including repackagers and relabelers. The FDA regulates 00612_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 00612_FLUKA 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 00612_FLUKA supplier is an individual or a company that provides 00612_FLUKA active pharmaceutical ingredient (API) or 00612_FLUKA finished formulations upon request. The 00612_FLUKA suppliers may include 00612_FLUKA API manufacturers, exporters, distributors and traders.
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A 00612_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 00612_FLUKA Certificate of Suitability (COS). The purpose of a 00612_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 00612_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 00612_FLUKA to their clients by showing that a 00612_FLUKA CEP has been issued for it. The manufacturer submits a 00612_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 00612_FLUKA CEP holder for the record. Additionally, the data presented in the 00612_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 00612_FLUKA DMF.
A 00612_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 00612_FLUKA CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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