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01 1Kanoria Chemicals & Industries Limited Distt. Sonebhadra IN
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01 1Lindane
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01 1India
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01 1Withdrawn by EDQM Failure to CEP procedure
Certificate Number : R0-CEP 2004-290 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2006-07-07
Type : Chemical
Substance Number : 772
43
PharmaCompass offers a list of gamma-BHC 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 gamma-BHC manufacturer or gamma-BHC supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred gamma-BHC manufacturer or gamma-BHC supplier.
PharmaCompass also assists you with knowing the gamma-BHC API Price utilized in the formulation of products. gamma-BHC API Price is not always fixed or binding as the gamma-BHC Price is obtained through a variety of data sources. The gamma-BHC Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kwell manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kwell, including repackagers and relabelers. The FDA regulates Kwell manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kwell 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 Kwell supplier is an individual or a company that provides Kwell active pharmaceutical ingredient (API) or Kwell finished formulations upon request. The Kwell suppliers may include Kwell API manufacturers, exporters, distributors and traders.
click here to find a list of Kwell suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Kwell CEP of the European Pharmacopoeia monograph is often referred to as a Kwell Certificate of Suitability (COS). The purpose of a Kwell CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Kwell EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Kwell to their clients by showing that a Kwell CEP has been issued for it. The manufacturer submits a Kwell CEP (COS) as part of the market authorization procedure, and it takes on the role of a Kwell CEP holder for the record. Additionally, the data presented in the Kwell CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Kwell DMF.
A Kwell CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Kwell 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 Kwell suppliers with CEP (COS) on PharmaCompass.
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