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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 0042AF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0042AF, including repackagers and relabelers. The FDA regulates 0042AF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0042AF 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 0042AF supplier is an individual or a company that provides 0042AF active pharmaceutical ingredient (API) or 0042AF finished formulations upon request. The 0042AF suppliers may include 0042AF API manufacturers, exporters, distributors and traders.
click here to find a list of 0042AF suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 0042AF DMF (Drug Master File) is a document detailing the whole manufacturing process of 0042AF active pharmaceutical ingredient (API) in detail. Different forms of 0042AF DMFs exist exist since differing nations have different regulations, such as 0042AF USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 0042AF DMF submitted to regulatory agencies in the US is known as a USDMF. 0042AF USDMF includes data on 0042AF's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 0042AF USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 0042AF suppliers with USDMF on PharmaCompass.
A 0042AF CEP of the European Pharmacopoeia monograph is often referred to as a 0042AF Certificate of Suitability (COS). The purpose of a 0042AF CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 0042AF EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 0042AF to their clients by showing that a 0042AF CEP has been issued for it. The manufacturer submits a 0042AF CEP (COS) as part of the market authorization procedure, and it takes on the role of a 0042AF CEP holder for the record. Additionally, the data presented in the 0042AF CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 0042AF DMF.
A 0042AF CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 0042AF 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 0042AF suppliers with CEP (COS) on PharmaCompass.
0042AF 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 0042AF 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 0042AF GMP manufacturer or 0042AF GMP API supplier for your needs.
A 0042AF CoA (Certificate of Analysis) is a formal document that attests to 0042AF's compliance with 0042AF specifications and serves as a tool for batch-level quality control.
0042AF CoA mostly includes findings from lab analyses of a specific batch. For each 0042AF 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.
0042AF may be tested according to a variety of international standards, such as European Pharmacopoeia (0042AF EP), 0042AF JP (Japanese Pharmacopeia) and the US Pharmacopoeia (0042AF USP).