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01 1Synteco S.p.A. San Martino Siccomario IT
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01 1Benfluorex hydrochloride
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01 1Italy
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01 1Expired
Certificate Number : R0-CEP 2002-092 - Rev 02
Status : Expired
Issue Date : 2005-06-02
Type : Chemical
Substance Number : 1601
99
PharmaCompass offers a list of Benfluorex 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 Benfluorex manufacturer or Benfluorex supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benfluorex manufacturer or Benfluorex supplier.
PharmaCompass also assists you with knowing the Benfluorex API Price utilized in the formulation of products. Benfluorex API Price is not always fixed or binding as the Benfluorex Price is obtained through a variety of data sources. The Benfluorex Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mediator manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mediator, including repackagers and relabelers. The FDA regulates Mediator manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mediator 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 Mediator supplier is an individual or a company that provides Mediator active pharmaceutical ingredient (API) or Mediator finished formulations upon request. The Mediator suppliers may include Mediator API manufacturers, exporters, distributors and traders.
click here to find a list of Mediator suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mediator CEP of the European Pharmacopoeia monograph is often referred to as a Mediator Certificate of Suitability (COS). The purpose of a Mediator CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Mediator EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Mediator to their clients by showing that a Mediator CEP has been issued for it. The manufacturer submits a Mediator CEP (COS) as part of the market authorization procedure, and it takes on the role of a Mediator CEP holder for the record. Additionally, the data presented in the Mediator CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Mediator DMF.
A Mediator CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Mediator 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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