Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
FDF
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
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]API Reference Price
API Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Related Excipient Companies
Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Parenteral
Topical
Market Place
ABOUT THIS PAGE
A Fospropofol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fospropofol, including repackagers and relabelers. The FDA regulates Fospropofol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fospropofol 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 Fospropofol supplier is an individual or a company that provides Fospropofol active pharmaceutical ingredient (API) or Fospropofol finished formulations upon request. The Fospropofol suppliers may include Fospropofol API manufacturers, exporters, distributors and traders.
click here to find a list of Fospropofol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fospropofol DMF (Drug Master File) is a document detailing the whole manufacturing process of Fospropofol active pharmaceutical ingredient (API) in detail. Different forms of Fospropofol DMFs exist exist since differing nations have different regulations, such as Fospropofol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fospropofol DMF submitted to regulatory agencies in the US is known as a USDMF. Fospropofol USDMF includes data on Fospropofol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fospropofol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fospropofol suppliers with USDMF on PharmaCompass.
Fospropofol 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 Fospropofol 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 Fospropofol GMP manufacturer or Fospropofol GMP API supplier for your needs.
A Fospropofol CoA (Certificate of Analysis) is a formal document that attests to Fospropofol's compliance with Fospropofol specifications and serves as a tool for batch-level quality control.
Fospropofol CoA mostly includes findings from lab analyses of a specific batch. For each Fospropofol 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.
Fospropofol may be tested according to a variety of international standards, such as European Pharmacopoeia (Fospropofol EP), Fospropofol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fospropofol USP).
LOOKING FOR A SUPPLIER?
