01 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
01 1Entecavir monohydrate, Process CZK
01 1China
01 1Valid
Entecavir Monohydrate, Process CZK
Certificate Number : CEP 2023-239 - Rev 00
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 2815
56
PharmaCompass offers a list of Entecavir Monohydrate 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 Entecavir Monohydrate manufacturer or Entecavir Monohydrate supplier for your needs.
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PharmaCompass also assists you with knowing the Entecavir Monohydrate API Price utilized in the formulation of products. Entecavir Monohydrate API Price is not always fixed or binding as the Entecavir Monohydrate Price is obtained through a variety of data sources. The Entecavir Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Entecavir Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Entecavir Monohydrate, including repackagers and relabelers. The FDA regulates Entecavir Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Entecavir Monohydrate 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 Entecavir Monohydrate supplier is an individual or a company that provides Entecavir Monohydrate active pharmaceutical ingredient (API) or Entecavir Monohydrate finished formulations upon request. The Entecavir Monohydrate suppliers may include Entecavir Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Entecavir Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Entecavir Monohydrate CEP of the European Pharmacopoeia monograph is often referred to as a Entecavir Monohydrate Certificate of Suitability (COS). The purpose of a Entecavir Monohydrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Entecavir Monohydrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Entecavir Monohydrate to their clients by showing that a Entecavir Monohydrate CEP has been issued for it. The manufacturer submits a Entecavir Monohydrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Entecavir Monohydrate CEP holder for the record. Additionally, the data presented in the Entecavir Monohydrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Entecavir Monohydrate DMF.
A Entecavir Monohydrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Entecavir Monohydrate 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 Entecavir Monohydrate suppliers with CEP (COS) on PharmaCompass.
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