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
02 1ICE S.P.A. Reggio Emilia IT
01 1Deoxycholic Acid
02 1Deoxycholic Acid and its derivatives, Product codes: 2808, 2316, 2317, 2828, 2007, 2015 and 2318
01 2Italy
01 2Valid
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.
Deoxycholic Acid And Its Derivatives, Product Co...
Certificate Number : R1-CEP 2001-331 - Rev 03
Status : Valid
Issue Date : 2020-06-05
Type : TSE
Substance Number :
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.
Certificate Number : R1-CEP 2000-335 - Rev 03
Status : Valid
Issue Date : 2017-03-14
Type : TSE
Substance Number :
73
PharmaCompass offers a list of Deoxycholic Acid 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 Deoxycholic Acid manufacturer or Deoxycholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deoxycholic Acid manufacturer or Deoxycholic Acid supplier.
PharmaCompass also assists you with knowing the Deoxycholic Acid API Price utilized in the formulation of products. Deoxycholic Acid API Price is not always fixed or binding as the Deoxycholic Acid Price is obtained through a variety of data sources. The Deoxycholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Degalol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Degalol, including repackagers and relabelers. The FDA regulates Degalol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Degalol 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 Degalol supplier is an individual or a company that provides Degalol active pharmaceutical ingredient (API) or Degalol finished formulations upon request. The Degalol suppliers may include Degalol API manufacturers, exporters, distributors and traders.
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A Degalol CEP of the European Pharmacopoeia monograph is often referred to as a Degalol Certificate of Suitability (COS). The purpose of a Degalol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Degalol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Degalol to their clients by showing that a Degalol CEP has been issued for it. The manufacturer submits a Degalol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Degalol CEP holder for the record. Additionally, the data presented in the Degalol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Degalol DMF.
A Degalol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Degalol 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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