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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
A Vindesine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vindesine Sulfate, including repackagers and relabelers. The FDA regulates Vindesine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vindesine Sulfate 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 Vindesine Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vindesine Sulfate supplier is an individual or a company that provides Vindesine Sulfate active pharmaceutical ingredient (API) or Vindesine Sulfate finished formulations upon request. The Vindesine Sulfate suppliers may include Vindesine Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Vindesine Sulfate 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 Vindesine Sulfate Drug Master File in Japan (Vindesine Sulfate JDMF) empowers Vindesine Sulfate 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 Vindesine Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Vindesine Sulfate 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 Vindesine Sulfate suppliers with JDMF on PharmaCompass.
Vindesine Sulfate 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 Vindesine Sulfate 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 Vindesine Sulfate GMP manufacturer or Vindesine Sulfate GMP API supplier for your needs.
A Vindesine Sulfate CoA (Certificate of Analysis) is a formal document that attests to Vindesine Sulfate's compliance with Vindesine Sulfate specifications and serves as a tool for batch-level quality control.
Vindesine Sulfate CoA mostly includes findings from lab analyses of a specific batch. For each Vindesine Sulfate 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.
Vindesine Sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (Vindesine Sulfate EP), Vindesine Sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vindesine Sulfate USP).
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