ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
01 1ICE S.P.A. Basaluzzo, Alessandria IT
01 1Chenodeoxycholic Acid, Product codes: 2608 - 2610 - 2611
01 1Italy
01 1Valid
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
Chenodeoxycholic Acid, Product Codes: 2608 - 261...
Certificate Number : R1-CEP 2003-238 - Rev 01
Status : Valid
Issue Date : 2020-06-05
Type : TSE
Substance Number : 1189
A Chenodeoxycholic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chenodeoxycholic Acid, including repackagers and relabelers. The FDA regulates Chenodeoxycholic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chenodeoxycholic Acid 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 Chenodeoxycholic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chenodeoxycholic Acid supplier is an individual or a company that provides Chenodeoxycholic Acid active pharmaceutical ingredient (API) or Chenodeoxycholic Acid finished formulations upon request. The Chenodeoxycholic Acid suppliers may include Chenodeoxycholic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Chenodeoxycholic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chenodeoxycholic Acid CEP of the European Pharmacopoeia monograph is often referred to as a Chenodeoxycholic Acid Certificate of Suitability (COS). The purpose of a Chenodeoxycholic Acid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Chenodeoxycholic Acid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Chenodeoxycholic Acid to their clients by showing that a Chenodeoxycholic Acid CEP has been issued for it. The manufacturer submits a Chenodeoxycholic Acid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Chenodeoxycholic Acid CEP holder for the record. Additionally, the data presented in the Chenodeoxycholic Acid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Chenodeoxycholic Acid DMF.
A Chenodeoxycholic Acid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Chenodeoxycholic Acid 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 Chenodeoxycholic Acid suppliers with CEP (COS) on PharmaCompass.
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