01 1HUANGSHAN BONSUN PHARMACEUTICALS CO., LTD. Shexian CN
02 1STAR-TECH & JRS SPECIALTY PRODUCTS CO., LTD. Chongqing CN
01 1Copovidone, K-value: 25.2-30.8
02 1Copovidone, K-value: 27.0-33.0
01 2China
01 2Valid
Copovidone, K-value: 27.0-33.0
Certificate Number : R0-CEP 2019-199 - Rev 00
Status : Valid
Issue Date : 2020-12-16
Type : Chemical
Substance Number : 891
Copovidone, K-value: 25.2-30.8
Certificate Number : R1-CEP 2014-365 - Rev 00
Status : Valid
Issue Date : 2021-02-16
Type : Chemical
Substance Number : 891
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PharmaCompass offers a list of Copovidone 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 Copovidone manufacturer or Copovidone supplier for your needs.
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PharmaCompass also assists you with knowing the Copovidone API Price utilized in the formulation of products. Copovidone API Price is not always fixed or binding as the Copovidone Price is obtained through a variety of data sources. The Copovidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ganex E 535 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ganex E 535, including repackagers and relabelers. The FDA regulates Ganex E 535 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ganex E 535 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Ganex E 535 supplier is an individual or a company that provides Ganex E 535 active pharmaceutical ingredient (API) or Ganex E 535 finished formulations upon request. The Ganex E 535 suppliers may include Ganex E 535 API manufacturers, exporters, distributors and traders.
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A Ganex E 535 CEP of the European Pharmacopoeia monograph is often referred to as a Ganex E 535 Certificate of Suitability (COS). The purpose of a Ganex E 535 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ganex E 535 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ganex E 535 to their clients by showing that a Ganex E 535 CEP has been issued for it. The manufacturer submits a Ganex E 535 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ganex E 535 CEP holder for the record. Additionally, the data presented in the Ganex E 535 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ganex E 535 DMF.
A Ganex E 535 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ganex E 535 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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