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PharmaCompass offers a list of Vitamin K1 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 Vitamin K1 manufacturer or Vitamin K1 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin K1 manufacturer or Vitamin K1 supplier.
PharmaCompass also assists you with knowing the Vitamin K1 API Price utilized in the formulation of products. Vitamin K1 API Price is not always fixed or binding as the Vitamin K1 Price is obtained through a variety of data sources. The Vitamin K1 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Phytonadione manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phytonadione, including repackagers and relabelers. The FDA regulates Phytonadione manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phytonadione 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 Phytonadione manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Phytonadione supplier is an individual or a company that provides Phytonadione active pharmaceutical ingredient (API) or Phytonadione finished formulations upon request. The Phytonadione suppliers may include Phytonadione API manufacturers, exporters, distributors and traders.
click here to find a list of Phytonadione 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 Phytonadione Drug Master File in Japan (Phytonadione JDMF) empowers Phytonadione 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 Phytonadione JDMF during the approval evaluation for pharmaceutical products. At the time of Phytonadione 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 Phytonadione suppliers with JDMF on PharmaCompass.
We have 4 companies offering Phytonadione
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