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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Global Sales Information
ABOUT THIS PAGE
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PharmaCompass offers a list of Vindesine Sulfate 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 Vindesine Sulfate manufacturer or Vindesine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vindesine Sulfate manufacturer or Vindesine Sulfate supplier.
PharmaCompass also assists you with knowing the Vindesine Sulfate API Price utilized in the formulation of products. Vindesine Sulfate API Price is not always fixed or binding as the Vindesine Sulfate Price is obtained through a variety of data sources. The Vindesine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eldesine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eldesine, including repackagers and relabelers. The FDA regulates Eldesine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eldesine 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 Eldesine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eldesine supplier is an individual or a company that provides Eldesine active pharmaceutical ingredient (API) or Eldesine finished formulations upon request. The Eldesine suppliers may include Eldesine API manufacturers, exporters, distributors and traders.
click here to find a list of Eldesine 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 Eldesine Drug Master File in Japan (Eldesine JDMF) empowers Eldesine 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 Eldesine JDMF during the approval evaluation for pharmaceutical products. At the time of Eldesine 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 Eldesine suppliers with JDMF on PharmaCompass.
Eldesine 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 Eldesine 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 Eldesine GMP manufacturer or Eldesine GMP API supplier for your needs.
A Eldesine CoA (Certificate of Analysis) is a formal document that attests to Eldesine's compliance with Eldesine specifications and serves as a tool for batch-level quality control.
Eldesine CoA mostly includes findings from lab analyses of a specific batch. For each Eldesine 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.
Eldesine may be tested according to a variety of international standards, such as European Pharmacopoeia (Eldesine EP), Eldesine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eldesine USP).
