01 1Kyongbo Pharmaceutical Co. , Ltd.
01 1Doxifluridine
01 1South Korea
Registration Number : 303MF10008
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2021-01-20
Latest Date of Registration : 2022-11-30
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PharmaCompass offers a list of Doxifluridine 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 Doxifluridine manufacturer or Doxifluridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxifluridine manufacturer or Doxifluridine supplier.
PharmaCompass also assists you with knowing the Doxifluridine API Price utilized in the formulation of products. Doxifluridine API Price is not always fixed or binding as the Doxifluridine Price is obtained through a variety of data sources. The Doxifluridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flutron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flutron, including repackagers and relabelers. The FDA regulates Flutron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flutron 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 Flutron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flutron supplier is an individual or a company that provides Flutron active pharmaceutical ingredient (API) or Flutron finished formulations upon request. The Flutron suppliers may include Flutron API manufacturers, exporters, distributors and traders.
click here to find a list of Flutron 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 Flutron Drug Master File in Japan (Flutron JDMF) empowers Flutron 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 Flutron JDMF during the approval evaluation for pharmaceutical products. At the time of Flutron 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 Flutron suppliers with JDMF on PharmaCompass.
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