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01 1PK CHEMICALS A/S KOGE DK
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01 1Malathion
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01 1Denmark
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01 1Withdrawn by Holder
Certificate Number : R0-CEP 2017-213 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2019-06-19
Type : Chemical
Substance Number : 1343
69
PharmaCompass offers a list of Malathion 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 Malathion manufacturer or Malathion supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Malathion manufacturer or Malathion supplier.
PharmaCompass also assists you with knowing the Malathion API Price utilized in the formulation of products. Malathion API Price is not always fixed or binding as the Malathion Price is obtained through a variety of data sources. The Malathion Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etiol, including repackagers and relabelers. The FDA regulates Etiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etiol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Etiol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etiol supplier is an individual or a company that provides Etiol active pharmaceutical ingredient (API) or Etiol finished formulations upon request. The Etiol suppliers may include Etiol API manufacturers, exporters, distributors and traders.
click here to find a list of Etiol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etiol CEP of the European Pharmacopoeia monograph is often referred to as a Etiol Certificate of Suitability (COS). The purpose of a Etiol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etiol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etiol to their clients by showing that a Etiol CEP has been issued for it. The manufacturer submits a Etiol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etiol CEP holder for the record. Additionally, the data presented in the Etiol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etiol DMF.
A Etiol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etiol 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 Etiol suppliers with CEP (COS) on PharmaCompass.