01 1MAGLE CHEMOSWED AB Malmö SE
01 1Isradipine
01 1Sweden
01 1Valid
Certificate Number : R1-CEP 2007-303 - Rev 03
Status : Valid
Issue Date : 2023-02-17
Type : Chemical
Substance Number : 2110
24
PharmaCompass offers a list of Isradipine 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 Isradipine manufacturer or Isradipine supplier for your needs.
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PharmaCompass also assists you with knowing the Isradipine API Price utilized in the formulation of products. Isradipine API Price is not always fixed or binding as the Isradipine Price is obtained through a variety of data sources. The Isradipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Icaz manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Icaz, including repackagers and relabelers. The FDA regulates Icaz manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Icaz 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 Icaz manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Icaz supplier is an individual or a company that provides Icaz active pharmaceutical ingredient (API) or Icaz finished formulations upon request. The Icaz suppliers may include Icaz API manufacturers, exporters, distributors and traders.
click here to find a list of Icaz suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Icaz CEP of the European Pharmacopoeia monograph is often referred to as a Icaz Certificate of Suitability (COS). The purpose of a Icaz CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Icaz EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Icaz to their clients by showing that a Icaz CEP has been issued for it. The manufacturer submits a Icaz CEP (COS) as part of the market authorization procedure, and it takes on the role of a Icaz CEP holder for the record. Additionally, the data presented in the Icaz CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Icaz DMF.
A Icaz CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Icaz 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 Icaz suppliers with CEP (COS) on PharmaCompass.
