01 1Ferak Berlin GmbH Berlin DE
02 1IMCD UK LIMITED Sutton GB
01 2Hexylresorcinol
01 1Germany
02 1Netherlands
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2002-073 - Rev 02
Status : Valid
Issue Date : 2016-11-10
Type : Chemical
Substance Number : 1437
Certificate Number : R0-CEP 2006-118 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2009-01-23
Type : Chemical
Substance Number : 1437
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PharmaCompass offers a list of Hexylresorcinol 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 Hexylresorcinol manufacturer or Hexylresorcinol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hexylresorcinol manufacturer or Hexylresorcinol supplier.
PharmaCompass also assists you with knowing the Hexylresorcinol API Price utilized in the formulation of products. Hexylresorcinol API Price is not always fixed or binding as the Hexylresorcinol Price is obtained through a variety of data sources. The Hexylresorcinol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Caprokol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Caprokol, including repackagers and relabelers. The FDA regulates Caprokol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Caprokol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Caprokol supplier is an individual or a company that provides Caprokol active pharmaceutical ingredient (API) or Caprokol finished formulations upon request. The Caprokol suppliers may include Caprokol API manufacturers, exporters, distributors and traders.
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A Caprokol CEP of the European Pharmacopoeia monograph is often referred to as a Caprokol Certificate of Suitability (COS). The purpose of a Caprokol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Caprokol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Caprokol to their clients by showing that a Caprokol CEP has been issued for it. The manufacturer submits a Caprokol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Caprokol CEP holder for the record. Additionally, the data presented in the Caprokol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Caprokol DMF.
A Caprokol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Caprokol 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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