Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
KDMF
0
VMF
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
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]
EU WC
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Digital Content
DATA COMPILATION #PharmaFlow
Market Place
ABOUT THIS PAGE
A Pemetrexed Tromethamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pemetrexed Tromethamine, including repackagers and relabelers. The FDA regulates Pemetrexed Tromethamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pemetrexed Tromethamine 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 Pemetrexed Tromethamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pemetrexed Tromethamine supplier is an individual or a company that provides Pemetrexed Tromethamine active pharmaceutical ingredient (API) or Pemetrexed Tromethamine finished formulations upon request. The Pemetrexed Tromethamine suppliers may include Pemetrexed Tromethamine API manufacturers, exporters, distributors and traders.
click here to find a list of Pemetrexed Tromethamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pemetrexed Tromethamine written confirmation (Pemetrexed Tromethamine WC) is an official document issued by a regulatory agency to a Pemetrexed Tromethamine manufacturer, verifying that the manufacturing facility of a Pemetrexed Tromethamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pemetrexed Tromethamine APIs or Pemetrexed Tromethamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Pemetrexed Tromethamine WC (written confirmation) as part of the regulatory process.
click here to find a list of Pemetrexed Tromethamine suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Pemetrexed Tromethamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pemetrexed Tromethamine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Pemetrexed Tromethamine as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Pemetrexed Tromethamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pemetrexed Tromethamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pemetrexed Tromethamine suppliers with NDC on PharmaCompass.
Pemetrexed Tromethamine 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 Pemetrexed Tromethamine 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 Pemetrexed Tromethamine GMP manufacturer or Pemetrexed Tromethamine GMP API supplier for your needs.
A Pemetrexed Tromethamine CoA (Certificate of Analysis) is a formal document that attests to Pemetrexed Tromethamine's compliance with Pemetrexed Tromethamine specifications and serves as a tool for batch-level quality control.
Pemetrexed Tromethamine CoA mostly includes findings from lab analyses of a specific batch. For each Pemetrexed Tromethamine 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.
Pemetrexed Tromethamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Pemetrexed Tromethamine EP), Pemetrexed Tromethamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pemetrexed Tromethamine USP).
LOOKING FOR A SUPPLIER?
