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01 1Zhejiang Charioteer Pharmaceutical Co., Ltd. Xianju CN
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01 1Ganciclovir
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01 1China
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01 1Valid
Certificate Number : R1-CEP 2013-123 - Rev 01
Status : Valid
Issue Date : 2019-06-20
Type : Chemical
Substance Number : 1752
33
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ganciclovir manufacturer or Ganciclovir supplier.
PharmaCompass also assists you with knowing the Ganciclovir API Price utilized in the formulation of products. Ganciclovir API Price is not always fixed or binding as the Ganciclovir Price is obtained through a variety of data sources. The Ganciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cymevene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymevene, including repackagers and relabelers. The FDA regulates Cymevene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymevene 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 Cymevene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cymevene supplier is an individual or a company that provides Cymevene active pharmaceutical ingredient (API) or Cymevene finished formulations upon request. The Cymevene suppliers may include Cymevene API manufacturers, exporters, distributors and traders.
click here to find a list of Cymevene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cymevene CEP of the European Pharmacopoeia monograph is often referred to as a Cymevene Certificate of Suitability (COS). The purpose of a Cymevene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cymevene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cymevene to their clients by showing that a Cymevene CEP has been issued for it. The manufacturer submits a Cymevene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cymevene CEP holder for the record. Additionally, the data presented in the Cymevene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cymevene DMF.
A Cymevene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cymevene 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 Cymevene suppliers with CEP (COS) on PharmaCompass.