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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 HFA-134-A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HFA-134-A, including repackagers and relabelers. The FDA regulates HFA-134-A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HFA-134-A 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 HFA-134-A supplier is an individual or a company that provides HFA-134-A active pharmaceutical ingredient (API) or HFA-134-A finished formulations upon request. The HFA-134-A suppliers may include HFA-134-A API manufacturers, exporters, distributors and traders.
click here to find a list of HFA-134-A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A HFA-134-A CEP of the European Pharmacopoeia monograph is often referred to as a HFA-134-A Certificate of Suitability (COS). The purpose of a HFA-134-A CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of HFA-134-A EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of HFA-134-A to their clients by showing that a HFA-134-A CEP has been issued for it. The manufacturer submits a HFA-134-A CEP (COS) as part of the market authorization procedure, and it takes on the role of a HFA-134-A CEP holder for the record. Additionally, the data presented in the HFA-134-A CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the HFA-134-A DMF.
A HFA-134-A CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. HFA-134-A 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 HFA-134-A suppliers with CEP (COS) on PharmaCompass.