01 1MESSER FRANCE Suresnes FR
02 1S.E. DE CARBUROS METALICOS, S.A. Cornellà de Llobregat ES
01 2Carbon dioxide
01 1France
02 1Spain
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2009-393 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2016-09-27
Type : Chemical
Substance Number : 375
Certificate Number : R0-CEP 2019-254 - Rev 00
Status : Valid
Issue Date : 2021-04-14
Type : Chemical
Substance Number : 375
86
PharmaCompass offers a list of Carbon Dioxide 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 Carbon Dioxide manufacturer or Carbon Dioxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carbon Dioxide manufacturer or Carbon Dioxide supplier.
PharmaCompass also assists you with knowing the Carbon Dioxide API Price utilized in the formulation of products. Carbon Dioxide API Price is not always fixed or binding as the Carbon Dioxide Price is obtained through a variety of data sources. The Carbon Dioxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dry ice manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dry ice, including repackagers and relabelers. The FDA regulates Dry ice manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dry ice API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Dry ice supplier is an individual or a company that provides Dry ice active pharmaceutical ingredient (API) or Dry ice finished formulations upon request. The Dry ice suppliers may include Dry ice API manufacturers, exporters, distributors and traders.
click here to find a list of Dry ice suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dry ice CEP of the European Pharmacopoeia monograph is often referred to as a Dry ice Certificate of Suitability (COS). The purpose of a Dry ice CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dry ice EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dry ice to their clients by showing that a Dry ice CEP has been issued for it. The manufacturer submits a Dry ice CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dry ice CEP holder for the record. Additionally, the data presented in the Dry ice CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dry ice DMF.
A Dry ice CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dry ice 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 Dry ice suppliers with CEP (COS) on PharmaCompass.
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