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 DXC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DXC, including repackagers and relabelers. The FDA regulates DXC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DXC 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 DXC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DXC supplier is an individual or a company that provides DXC active pharmaceutical ingredient (API) or DXC finished formulations upon request. The DXC suppliers may include DXC API manufacturers, exporters, distributors and traders.
click here to find a list of DXC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DXC CEP of the European Pharmacopoeia monograph is often referred to as a DXC Certificate of Suitability (COS). The purpose of a DXC CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DXC EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DXC to their clients by showing that a DXC CEP has been issued for it. The manufacturer submits a DXC CEP (COS) as part of the market authorization procedure, and it takes on the role of a DXC CEP holder for the record. Additionally, the data presented in the DXC CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DXC DMF.
A DXC CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DXC 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 DXC suppliers with CEP (COS) on PharmaCompass.
