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