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Status : Withdrawn by EDQM Failure to CEP pro...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