01 1Zhejiang Charioteer Pharmaceutical Co., Ltd. Xianju CN
01 1Ganciclovir
01 1China
01 1Valid
Certificate Number : R1-CEP 2013-123 - Rev 01
Status : Valid
Issue Date : 2019-06-20
Type : Chemical
Substance Number : 1752
17
PharmaCompass offers a list of Ganciclovir 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 Ganciclovir manufacturer or Ganciclovir supplier for your needs.
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A Cytovene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytovene, including repackagers and relabelers. The FDA regulates Cytovene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytovene 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 Cytovene supplier is an individual or a company that provides Cytovene active pharmaceutical ingredient (API) or Cytovene finished formulations upon request. The Cytovene suppliers may include Cytovene API manufacturers, exporters, distributors and traders.
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A Cytovene CEP of the European Pharmacopoeia monograph is often referred to as a Cytovene Certificate of Suitability (COS). The purpose of a Cytovene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cytovene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cytovene to their clients by showing that a Cytovene CEP has been issued for it. The manufacturer submits a Cytovene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cytovene CEP holder for the record. Additionally, the data presented in the Cytovene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cytovene DMF.
A Cytovene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cytovene 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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