Synopsis
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NDC API
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VMF
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EDQM
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USP
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JP
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Europe
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South Africa
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DRUG PRODUCT COMPOSITIONS
US Medicaid
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
About the Company : Mankind Pharma, came into existence in 1986. In 1991, the company was formed into a legal corporation. However, it actively started working as a fully integrated pharmaceutical com...
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
About the Company : Founded in 1984, DRL is well-known for its generic APIs and its track record in drug product development. It is one of the earliest pharma API manufacturers with a diverse portfoli...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Drugs in Development
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PharmaCompass offers a list of Perfluorohexyloctane 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 Perfluorohexyloctane manufacturer or Perfluorohexyloctane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perfluorohexyloctane manufacturer or Perfluorohexyloctane supplier.
PharmaCompass also assists you with knowing the Perfluorohexyloctane API Price utilized in the formulation of products. Perfluorohexyloctane API Price is not always fixed or binding as the Perfluorohexyloctane Price is obtained through a variety of data sources. The Perfluorohexyloctane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1-(Perfluorohexyl)Octane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1-(Perfluorohexyl)Octane, including repackagers and relabelers. The FDA regulates 1-(Perfluorohexyl)Octane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1-(Perfluorohexyl)Octane API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 1-(Perfluorohexyl)Octane manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1-(Perfluorohexyl)Octane supplier is an individual or a company that provides 1-(Perfluorohexyl)Octane active pharmaceutical ingredient (API) or 1-(Perfluorohexyl)Octane finished formulations upon request. The 1-(Perfluorohexyl)Octane suppliers may include 1-(Perfluorohexyl)Octane API manufacturers, exporters, distributors and traders.
click here to find a list of 1-(Perfluorohexyl)Octane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1-(Perfluorohexyl)Octane DMF (Drug Master File) is a document detailing the whole manufacturing process of 1-(Perfluorohexyl)Octane active pharmaceutical ingredient (API) in detail. Different forms of 1-(Perfluorohexyl)Octane DMFs exist exist since differing nations have different regulations, such as 1-(Perfluorohexyl)Octane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1-(Perfluorohexyl)Octane DMF submitted to regulatory agencies in the US is known as a USDMF. 1-(Perfluorohexyl)Octane USDMF includes data on 1-(Perfluorohexyl)Octane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1-(Perfluorohexyl)Octane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1-(Perfluorohexyl)Octane suppliers with USDMF on PharmaCompass.
1-(Perfluorohexyl)Octane 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-(Perfluorohexyl)Octane 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-(Perfluorohexyl)Octane GMP manufacturer or 1-(Perfluorohexyl)Octane GMP API supplier for your needs.
A 1-(Perfluorohexyl)Octane CoA (Certificate of Analysis) is a formal document that attests to 1-(Perfluorohexyl)Octane's compliance with 1-(Perfluorohexyl)Octane specifications and serves as a tool for batch-level quality control.
1-(Perfluorohexyl)Octane CoA mostly includes findings from lab analyses of a specific batch. For each 1-(Perfluorohexyl)Octane 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-(Perfluorohexyl)Octane may be tested according to a variety of international standards, such as European Pharmacopoeia (1-(Perfluorohexyl)Octane EP), 1-(Perfluorohexyl)Octane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (1-(Perfluorohexyl)Octane USP).
