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01 1SRF LIMITED Dahej IN
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01 1Norflurane
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01 1India
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01 1Valid
Certificate Number : R0-CEP 2018-195 - Rev 00
Status : Valid
Issue Date : 2020-05-20
Type : Chemical
Substance Number : 2257
96
PharmaCompass offers a list of 1,1,1,2-Tetrafluoroethane 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 1,1,1,2-Tetrafluoroethane manufacturer or 1,1,1,2-Tetrafluoroethane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 1,1,1,2-Tetrafluoroethane manufacturer or 1,1,1,2-Tetrafluoroethane supplier.
PharmaCompass also assists you with knowing the 1,1,1,2-Tetrafluoroethane API Price utilized in the formulation of products. 1,1,1,2-Tetrafluoroethane API Price is not always fixed or binding as the 1,1,1,2-Tetrafluoroethane Price is obtained through a variety of data sources. The 1,1,1,2-Tetrafluoroethane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CF3CH2F manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CF3CH2F, including repackagers and relabelers. The FDA regulates CF3CH2F manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CF3CH2F 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 CF3CH2F supplier is an individual or a company that provides CF3CH2F active pharmaceutical ingredient (API) or CF3CH2F finished formulations upon request. The CF3CH2F suppliers may include CF3CH2F API manufacturers, exporters, distributors and traders.
click here to find a list of CF3CH2F suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CF3CH2F CEP of the European Pharmacopoeia monograph is often referred to as a CF3CH2F Certificate of Suitability (COS). The purpose of a CF3CH2F CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CF3CH2F EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CF3CH2F to their clients by showing that a CF3CH2F CEP has been issued for it. The manufacturer submits a CF3CH2F CEP (COS) as part of the market authorization procedure, and it takes on the role of a CF3CH2F CEP holder for the record. Additionally, the data presented in the CF3CH2F CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CF3CH2F DMF.
A CF3CH2F CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CF3CH2F 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 CF3CH2F suppliers with CEP (COS) on PharmaCompass.