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