01 1KATWIJK CHEMIE BV Katwijk ZH NL
01 1Ethosuximide
01 1Netherlands
01 1Valid
Certificate Number : R1-CEP 2009-022 - Rev 04
Status : Valid
Issue Date : 2018-05-29
Type : Chemical
Substance Number : 764
100
PharmaCompass offers a list of Ethosuximide 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 Ethosuximide manufacturer or Ethosuximide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethosuximide manufacturer or Ethosuximide supplier.
PharmaCompass also assists you with knowing the Ethosuximide API Price utilized in the formulation of products. Ethosuximide API Price is not always fixed or binding as the Ethosuximide Price is obtained through a variety of data sources. The Ethosuximide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CI 366 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI 366, including repackagers and relabelers. The FDA regulates CI 366 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI 366 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 CI 366 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CI 366 supplier is an individual or a company that provides CI 366 active pharmaceutical ingredient (API) or CI 366 finished formulations upon request. The CI 366 suppliers may include CI 366 API manufacturers, exporters, distributors and traders.
click here to find a list of CI 366 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CI 366 CEP of the European Pharmacopoeia monograph is often referred to as a CI 366 Certificate of Suitability (COS). The purpose of a CI 366 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CI 366 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CI 366 to their clients by showing that a CI 366 CEP has been issued for it. The manufacturer submits a CI 366 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CI 366 CEP holder for the record. Additionally, the data presented in the CI 366 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CI 366 DMF.
A CI 366 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CI 366 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 CI 366 suppliers with CEP (COS) on PharmaCompass.
