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