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01 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
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01 1Entecavir monohydrate, Process CZK
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01 1China
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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
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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 MP-1495 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MP-1495, including repackagers and relabelers. The FDA regulates MP-1495 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MP-1495 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 MP-1495 supplier is an individual or a company that provides MP-1495 active pharmaceutical ingredient (API) or MP-1495 finished formulations upon request. The MP-1495 suppliers may include MP-1495 API manufacturers, exporters, distributors and traders.
click here to find a list of MP-1495 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MP-1495 CEP of the European Pharmacopoeia monograph is often referred to as a MP-1495 Certificate of Suitability (COS). The purpose of a MP-1495 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MP-1495 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MP-1495 to their clients by showing that a MP-1495 CEP has been issued for it. The manufacturer submits a MP-1495 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MP-1495 CEP holder for the record. Additionally, the data presented in the MP-1495 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MP-1495 DMF.
A MP-1495 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MP-1495 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 MP-1495 suppliers with CEP (COS) on PharmaCompass.
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