Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
Europe
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
NEWS #PharmaBuzz
Global Sales Information
Market Place
ABOUT THIS PAGE
86
PharmaCompass offers a list of Ferumoxytol 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 Ferumoxytol manufacturer or Ferumoxytol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferumoxytol manufacturer or Ferumoxytol supplier.
PharmaCompass also assists you with knowing the Ferumoxytol API Price utilized in the formulation of products. Ferumoxytol API Price is not always fixed or binding as the Ferumoxytol Price is obtained through a variety of data sources. The Ferumoxytol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytogen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytogen, including repackagers and relabelers. The FDA regulates Cytogen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytogen 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 Cytogen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytogen supplier is an individual or a company that provides Cytogen active pharmaceutical ingredient (API) or Cytogen finished formulations upon request. The Cytogen suppliers may include Cytogen API manufacturers, exporters, distributors and traders.
click here to find a list of Cytogen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cytogen DMF (Drug Master File) is a document detailing the whole manufacturing process of Cytogen active pharmaceutical ingredient (API) in detail. Different forms of Cytogen DMFs exist exist since differing nations have different regulations, such as Cytogen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cytogen DMF submitted to regulatory agencies in the US is known as a USDMF. Cytogen USDMF includes data on Cytogen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cytogen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cytogen suppliers with USDMF on PharmaCompass.
Cytogen 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 Cytogen 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 Cytogen GMP manufacturer or Cytogen GMP API supplier for your needs.
A Cytogen CoA (Certificate of Analysis) is a formal document that attests to Cytogen's compliance with Cytogen specifications and serves as a tool for batch-level quality control.
Cytogen CoA mostly includes findings from lab analyses of a specific batch. For each Cytogen 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.
Cytogen may be tested according to a variety of international standards, such as European Pharmacopoeia (Cytogen EP), Cytogen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cytogen USP).
