01 1OLON S.P.A. Rodano IT
01 1Mefloquine hydrochloride
01 1Italy
01 1Valid
Certificate Number : CEP 2011-099 - Rev 05
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 1241
77
PharmaCompass offers a list of Mefloquine 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 Mefloquine manufacturer or Mefloquine supplier for your needs.
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PharmaCompass also assists you with knowing the Mefloquine API Price utilized in the formulation of products. Mefloquine API Price is not always fixed or binding as the Mefloquine Price is obtained through a variety of data sources. The Mefloquine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-1430 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-1430, including repackagers and relabelers. The FDA regulates CS-1430 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-1430 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 CS-1430 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-1430 supplier is an individual or a company that provides CS-1430 active pharmaceutical ingredient (API) or CS-1430 finished formulations upon request. The CS-1430 suppliers may include CS-1430 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-1430 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CS-1430 CEP of the European Pharmacopoeia monograph is often referred to as a CS-1430 Certificate of Suitability (COS). The purpose of a CS-1430 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CS-1430 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CS-1430 to their clients by showing that a CS-1430 CEP has been issued for it. The manufacturer submits a CS-1430 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CS-1430 CEP holder for the record. Additionally, the data presented in the CS-1430 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CS-1430 DMF.
A CS-1430 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CS-1430 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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