Synopsis
0
USDMF
0
CEP/COS
0
KDMF
0
NDC API
0
VMF
0
FDF
0
FDF Dossiers
0
FDA Orange Book
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
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
Jai Radhe Sales is your partner for all your sourcing needs.
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
EU WC
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 Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Digital Content
NEWS #PharmaBuzz
Market Place
ABOUT THIS PAGE
A Fosfomycin Calcium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosfomycin Calcium, including repackagers and relabelers. The FDA regulates Fosfomycin Calcium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosfomycin Calcium 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 Fosfomycin Calcium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fosfomycin Calcium supplier is an individual or a company that provides Fosfomycin Calcium active pharmaceutical ingredient (API) or Fosfomycin Calcium finished formulations upon request. The Fosfomycin Calcium suppliers may include Fosfomycin Calcium API manufacturers, exporters, distributors and traders.
click here to find a list of Fosfomycin Calcium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Fosfomycin Calcium Drug Master File in Japan (Fosfomycin Calcium JDMF) empowers Fosfomycin Calcium API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Fosfomycin Calcium JDMF during the approval evaluation for pharmaceutical products. At the time of Fosfomycin Calcium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Fosfomycin Calcium suppliers with JDMF on PharmaCompass.
A Fosfomycin Calcium written confirmation (Fosfomycin Calcium WC) is an official document issued by a regulatory agency to a Fosfomycin Calcium manufacturer, verifying that the manufacturing facility of a Fosfomycin Calcium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fosfomycin Calcium APIs or Fosfomycin Calcium finished pharmaceutical products to another nation, regulatory agencies frequently require a Fosfomycin Calcium WC (written confirmation) as part of the regulatory process.
click here to find a list of Fosfomycin Calcium suppliers with Written Confirmation (WC) on PharmaCompass.
Fosfomycin Calcium 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 Fosfomycin Calcium 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 Fosfomycin Calcium GMP manufacturer or Fosfomycin Calcium GMP API supplier for your needs.
A Fosfomycin Calcium CoA (Certificate of Analysis) is a formal document that attests to Fosfomycin Calcium's compliance with Fosfomycin Calcium specifications and serves as a tool for batch-level quality control.
Fosfomycin Calcium CoA mostly includes findings from lab analyses of a specific batch. For each Fosfomycin Calcium 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.
Fosfomycin Calcium may be tested according to a variety of international standards, such as European Pharmacopoeia (Fosfomycin Calcium EP), Fosfomycin Calcium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fosfomycin Calcium USP).
LOOKING FOR A SUPPLIER?
