01 1IPCA LABORATORIES LIMITED Mumbai IN
01 1Chloroquine Phosphate
01 1India
01 1Valid
Certificate Number : CEP 2005-177 - Rev 02
Status : Valid
Issue Date : 2024-12-13
Type : Chemical
Substance Number : 544
94
PharmaCompass offers a list of Chloroquine Phosphate 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 Chloroquine Phosphate manufacturer or Chloroquine Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chloroquine Phosphate manufacturer or Chloroquine Phosphate supplier.
PharmaCompass also assists you with knowing the Chloroquine Phosphate API Price utilized in the formulation of products. Chloroquine Phosphate API Price is not always fixed or binding as the Chloroquine Phosphate Price is obtained through a variety of data sources. The Chloroquine Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tanakene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tanakene, including repackagers and relabelers. The FDA regulates Tanakene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tanakene 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 Tanakene supplier is an individual or a company that provides Tanakene active pharmaceutical ingredient (API) or Tanakene finished formulations upon request. The Tanakene suppliers may include Tanakene API manufacturers, exporters, distributors and traders.
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A Tanakene CEP of the European Pharmacopoeia monograph is often referred to as a Tanakene Certificate of Suitability (COS). The purpose of a Tanakene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tanakene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tanakene to their clients by showing that a Tanakene CEP has been issued for it. The manufacturer submits a Tanakene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tanakene CEP holder for the record. Additionally, the data presented in the Tanakene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tanakene DMF.
A Tanakene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tanakene 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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