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PharmaCompass offers a list of Fluorouracil 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 Fluorouracil manufacturer or Fluorouracil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluorouracil manufacturer or Fluorouracil supplier.
PharmaCompass also assists you with knowing the Fluorouracil API Price utilized in the formulation of products. Fluorouracil API Price is not always fixed or binding as the Fluorouracil Price is obtained through a variety of data sources. The Fluorouracil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1004-03-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1004-03-1, including repackagers and relabelers. The FDA regulates 1004-03-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1004-03-1 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 1004-03-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1004-03-1 supplier is an individual or a company that provides 1004-03-1 active pharmaceutical ingredient (API) or 1004-03-1 finished formulations upon request. The 1004-03-1 suppliers may include 1004-03-1 API manufacturers, exporters, distributors and traders.
click here to find a list of 1004-03-1 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 1004-03-1 Drug Master File in Japan (1004-03-1 JDMF) empowers 1004-03-1 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 1004-03-1 JDMF during the approval evaluation for pharmaceutical products. At the time of 1004-03-1 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 1004-03-1 suppliers with JDMF on PharmaCompass.
We have 2 companies offering 1004-03-1
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