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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 1,1,1,2-Tetrafluoroethane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1,1,1,2-Tetrafluoroethane, including repackagers and relabelers. The FDA regulates 1,1,1,2-Tetrafluoroethane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1,1,1,2-Tetrafluoroethane 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 1,1,1,2-Tetrafluoroethane supplier is an individual or a company that provides 1,1,1,2-Tetrafluoroethane active pharmaceutical ingredient (API) or 1,1,1,2-Tetrafluoroethane finished formulations upon request. The 1,1,1,2-Tetrafluoroethane suppliers may include 1,1,1,2-Tetrafluoroethane API manufacturers, exporters, distributors and traders.
click here to find a list of 1,1,1,2-Tetrafluoroethane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1,1,1,2-Tetrafluoroethane DMF (Drug Master File) is a document detailing the whole manufacturing process of 1,1,1,2-Tetrafluoroethane active pharmaceutical ingredient (API) in detail. Different forms of 1,1,1,2-Tetrafluoroethane DMFs exist exist since differing nations have different regulations, such as 1,1,1,2-Tetrafluoroethane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1,1,1,2-Tetrafluoroethane DMF submitted to regulatory agencies in the US is known as a USDMF. 1,1,1,2-Tetrafluoroethane USDMF includes data on 1,1,1,2-Tetrafluoroethane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1,1,1,2-Tetrafluoroethane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1,1,1,2-Tetrafluoroethane suppliers with USDMF on PharmaCompass.
A 1,1,1,2-Tetrafluoroethane CEP of the European Pharmacopoeia monograph is often referred to as a 1,1,1,2-Tetrafluoroethane Certificate of Suitability (COS). The purpose of a 1,1,1,2-Tetrafluoroethane CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 1,1,1,2-Tetrafluoroethane EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 1,1,1,2-Tetrafluoroethane to their clients by showing that a 1,1,1,2-Tetrafluoroethane CEP has been issued for it. The manufacturer submits a 1,1,1,2-Tetrafluoroethane CEP (COS) as part of the market authorization procedure, and it takes on the role of a 1,1,1,2-Tetrafluoroethane CEP holder for the record. Additionally, the data presented in the 1,1,1,2-Tetrafluoroethane CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 1,1,1,2-Tetrafluoroethane DMF.
A 1,1,1,2-Tetrafluoroethane CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 1,1,1,2-Tetrafluoroethane 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 1,1,1,2-Tetrafluoroethane suppliers with CEP (COS) on PharmaCompass.
1,1,1,2-Tetrafluoroethane Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of 1,1,1,2-Tetrafluoroethane GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right 1,1,1,2-Tetrafluoroethane GMP manufacturer or 1,1,1,2-Tetrafluoroethane GMP API supplier for your needs.
A 1,1,1,2-Tetrafluoroethane CoA (Certificate of Analysis) is a formal document that attests to 1,1,1,2-Tetrafluoroethane's compliance with 1,1,1,2-Tetrafluoroethane specifications and serves as a tool for batch-level quality control.
1,1,1,2-Tetrafluoroethane CoA mostly includes findings from lab analyses of a specific batch. For each 1,1,1,2-Tetrafluoroethane CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
1,1,1,2-Tetrafluoroethane may be tested according to a variety of international standards, such as European Pharmacopoeia (1,1,1,2-Tetrafluoroethane EP), 1,1,1,2-Tetrafluoroethane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1,1,1,2-Tetrafluoroethane USP).