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Status : Withdrawn by Holder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