Synopsis
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]
USDMF
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/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
INTERMEDIATE SUPPLIERS
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
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
69
PharmaCompass offers a list of Etofenamate 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 Etofenamate manufacturer or Etofenamate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etofenamate manufacturer or Etofenamate supplier.
PharmaCompass also assists you with knowing the Etofenamate API Price utilized in the formulation of products. Etofenamate API Price is not always fixed or binding as the Etofenamate Price is obtained through a variety of data sources. The Etofenamate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Traumon Gel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Traumon Gel, including repackagers and relabelers. The FDA regulates Traumon Gel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Traumon Gel 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 Traumon Gel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Traumon Gel supplier is an individual or a company that provides Traumon Gel active pharmaceutical ingredient (API) or Traumon Gel finished formulations upon request. The Traumon Gel suppliers may include Traumon Gel API manufacturers, exporters, distributors and traders.
click here to find a list of Traumon Gel suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Traumon Gel DMF (Drug Master File) is a document detailing the whole manufacturing process of Traumon Gel active pharmaceutical ingredient (API) in detail. Different forms of Traumon Gel DMFs exist exist since differing nations have different regulations, such as Traumon Gel USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Traumon Gel DMF submitted to regulatory agencies in the US is known as a USDMF. Traumon Gel USDMF includes data on Traumon Gel's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Traumon Gel USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Traumon Gel suppliers with USDMF on PharmaCompass.
A Traumon Gel CEP of the European Pharmacopoeia monograph is often referred to as a Traumon Gel Certificate of Suitability (COS). The purpose of a Traumon Gel CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Traumon Gel EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Traumon Gel to their clients by showing that a Traumon Gel CEP has been issued for it. The manufacturer submits a Traumon Gel CEP (COS) as part of the market authorization procedure, and it takes on the role of a Traumon Gel CEP holder for the record. Additionally, the data presented in the Traumon Gel CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Traumon Gel DMF.
A Traumon Gel CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Traumon Gel 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 Traumon Gel suppliers with CEP (COS) on PharmaCompass.
A Traumon Gel written confirmation (Traumon Gel WC) is an official document issued by a regulatory agency to a Traumon Gel manufacturer, verifying that the manufacturing facility of a Traumon Gel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Traumon Gel APIs or Traumon Gel finished pharmaceutical products to another nation, regulatory agencies frequently require a Traumon Gel WC (written confirmation) as part of the regulatory process.
click here to find a list of Traumon Gel suppliers with Written Confirmation (WC) on PharmaCompass.
Traumon Gel 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 Traumon Gel 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 Traumon Gel GMP manufacturer or Traumon Gel GMP API supplier for your needs.
A Traumon Gel CoA (Certificate of Analysis) is a formal document that attests to Traumon Gel's compliance with Traumon Gel specifications and serves as a tool for batch-level quality control.
Traumon Gel CoA mostly includes findings from lab analyses of a specific batch. For each Traumon Gel 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.
Traumon Gel may be tested according to a variety of international standards, such as European Pharmacopoeia (Traumon Gel EP), Traumon Gel JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Traumon Gel USP).
