Synopsis
0
USDMF
0
JDMF
0
KDMF
0
NDC API
0
VMF
0
FDA Orange Book
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
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]
CEP/COS
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 
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
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Ethamsylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethamsylate, including repackagers and relabelers. The FDA regulates Ethamsylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethamsylate 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 Ethamsylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethamsylate supplier is an individual or a company that provides Ethamsylate active pharmaceutical ingredient (API) or Ethamsylate finished formulations upon request. The Ethamsylate suppliers may include Ethamsylate API manufacturers, exporters, distributors and traders.
click here to find a list of Ethamsylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethamsylate CEP of the European Pharmacopoeia monograph is often referred to as a Ethamsylate Certificate of Suitability (COS). The purpose of a Ethamsylate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ethamsylate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ethamsylate to their clients by showing that a Ethamsylate CEP has been issued for it. The manufacturer submits a Ethamsylate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ethamsylate CEP holder for the record. Additionally, the data presented in the Ethamsylate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ethamsylate DMF.
A Ethamsylate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ethamsylate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Ethamsylate suppliers with CEP (COS) on PharmaCompass.
A Ethamsylate written confirmation (Ethamsylate WC) is an official document issued by a regulatory agency to a Ethamsylate manufacturer, verifying that the manufacturing facility of a Ethamsylate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ethamsylate APIs or Ethamsylate finished pharmaceutical products to another nation, regulatory agencies frequently require a Ethamsylate WC (written confirmation) as part of the regulatory process.
click here to find a list of Ethamsylate suppliers with Written Confirmation (WC) on PharmaCompass.
Ethamsylate 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 Ethamsylate 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 Ethamsylate GMP manufacturer or Ethamsylate GMP API supplier for your needs.
A Ethamsylate CoA (Certificate of Analysis) is a formal document that attests to Ethamsylate's compliance with Ethamsylate specifications and serves as a tool for batch-level quality control.
Ethamsylate CoA mostly includes findings from lab analyses of a specific batch. For each Ethamsylate 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.
Ethamsylate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ethamsylate EP), Ethamsylate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ethamsylate USP).
LOOKING FOR A SUPPLIER?
