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01 1JANSSEN PHARMACEUTICA NV Beerse BE
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01 1Clazuril for veterinary use
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01 1Belgium
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01 1Expired
Certificate Number : R0-CEP 2004-145 - Rev 00
Status : Expired
Issue Date : 2006-05-15
Type : Chemical
Substance Number : 1714
59
PharmaCompass offers a list of Clazuril 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 Clazuril manufacturer or Clazuril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clazuril manufacturer or Clazuril supplier.
PharmaCompass also assists you with knowing the Clazuril API Price utilized in the formulation of products. Clazuril API Price is not always fixed or binding as the Clazuril Price is obtained through a variety of data sources. The Clazuril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clazuril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clazuril, including repackagers and relabelers. The FDA regulates Clazuril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clazuril 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 Clazuril supplier is an individual or a company that provides Clazuril active pharmaceutical ingredient (API) or Clazuril finished formulations upon request. The Clazuril suppliers may include Clazuril API manufacturers, exporters, distributors and traders.
click here to find a list of Clazuril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clazuril CEP of the European Pharmacopoeia monograph is often referred to as a Clazuril Certificate of Suitability (COS). The purpose of a Clazuril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clazuril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clazuril to their clients by showing that a Clazuril CEP has been issued for it. The manufacturer submits a Clazuril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clazuril CEP holder for the record. Additionally, the data presented in the Clazuril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clazuril DMF.
A Clazuril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clazuril 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 Clazuril suppliers with CEP (COS) on PharmaCompass.
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