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01 1CSL BEHRING GMBH Marburg DE
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01 1Water for injections, Sterilised
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01 1U.S.A
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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 GTE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GTE, including repackagers and relabelers. The FDA regulates GTE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GTE 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 GTE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A GTE supplier is an individual or a company that provides GTE active pharmaceutical ingredient (API) or GTE finished formulations upon request. The GTE suppliers may include GTE API manufacturers, exporters, distributors and traders.
click here to find a list of GTE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A GTE CEP of the European Pharmacopoeia monograph is often referred to as a GTE Certificate of Suitability (COS). The purpose of a GTE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of GTE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of GTE to their clients by showing that a GTE CEP has been issued for it. The manufacturer submits a GTE CEP (COS) as part of the market authorization procedure, and it takes on the role of a GTE CEP holder for the record. Additionally, the data presented in the GTE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the GTE DMF.
A GTE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. GTE 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 GTE suppliers with CEP (COS) on PharmaCompass.