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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Status : Withdrawn by EDQM Failure to CEP pro...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
50
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.
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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 Lacco HI lin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lacco HI lin, including repackagers and relabelers. The FDA regulates Lacco HI lin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lacco HI lin 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 Lacco HI lin supplier is an individual or a company that provides Lacco HI lin active pharmaceutical ingredient (API) or Lacco HI lin finished formulations upon request. The Lacco HI lin suppliers may include Lacco HI lin API manufacturers, exporters, distributors and traders.
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A Lacco HI lin CEP of the European Pharmacopoeia monograph is often referred to as a Lacco HI lin Certificate of Suitability (COS). The purpose of a Lacco HI lin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lacco HI lin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lacco HI lin to their clients by showing that a Lacco HI lin CEP has been issued for it. The manufacturer submits a Lacco HI lin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lacco HI lin CEP holder for the record. Additionally, the data presented in the Lacco HI lin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lacco HI lin DMF.
A Lacco HI lin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lacco HI lin 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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