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PharmaCompass offers a list of Perfluorodichlorooctane 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 Perfluorodichlorooctane manufacturer or Perfluorodichlorooctane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perfluorodichlorooctane manufacturer or Perfluorodichlorooctane supplier.
PharmaCompass also assists you with knowing the Perfluorodichlorooctane API Price utilized in the formulation of products. Perfluorodichlorooctane API Price is not always fixed or binding as the Perfluorodichlorooctane Price is obtained through a variety of data sources. The Perfluorodichlorooctane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Perfluorodichlorooctane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perfluorodichlorooctane, including repackagers and relabelers. The FDA regulates Perfluorodichlorooctane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perfluorodichlorooctane 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 Perfluorodichlorooctane supplier is an individual or a company that provides Perfluorodichlorooctane active pharmaceutical ingredient (API) or Perfluorodichlorooctane finished formulations upon request. The Perfluorodichlorooctane suppliers may include Perfluorodichlorooctane API manufacturers, exporters, distributors and traders.
click here to find a list of Perfluorodichlorooctane suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Perfluorodichlorooctane DMF (Drug Master File) is a document detailing the whole manufacturing process of Perfluorodichlorooctane active pharmaceutical ingredient (API) in detail. Different forms of Perfluorodichlorooctane DMFs exist exist since differing nations have different regulations, such as Perfluorodichlorooctane USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Perfluorodichlorooctane DMF submitted to regulatory agencies in the US is known as a USDMF. Perfluorodichlorooctane USDMF includes data on Perfluorodichlorooctane's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Perfluorodichlorooctane USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Perfluorodichlorooctane suppliers with USDMF on PharmaCompass.
Perfluorodichlorooctane 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 Perfluorodichlorooctane 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 Perfluorodichlorooctane GMP manufacturer or Perfluorodichlorooctane GMP API supplier for your needs.
A Perfluorodichlorooctane CoA (Certificate of Analysis) is a formal document that attests to Perfluorodichlorooctane's compliance with Perfluorodichlorooctane specifications and serves as a tool for batch-level quality control.
Perfluorodichlorooctane CoA mostly includes findings from lab analyses of a specific batch. For each Perfluorodichlorooctane 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.
Perfluorodichlorooctane may be tested according to a variety of international standards, such as European Pharmacopoeia (Perfluorodichlorooctane EP), Perfluorodichlorooctane JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Perfluorodichlorooctane USP).