01 1LEO Pharma A/S
01 1Fusidic acid sodium
01 1Denmark
Registration Number : 218MF10952
Registrant's Address : Industryparken 55, DK-2750 Ballerup
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2019-09-26
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PharmaCompass offers a list of Sodium Fusidate 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 Sodium Fusidate manufacturer or Sodium Fusidate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Fusidate manufacturer or Sodium Fusidate supplier.
PharmaCompass also assists you with knowing the Sodium Fusidate API Price utilized in the formulation of products. Sodium Fusidate API Price is not always fixed or binding as the Sodium Fusidate Price is obtained through a variety of data sources. The Sodium Fusidate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fusin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fusin, including repackagers and relabelers. The FDA regulates Fusin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fusin 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 Fusin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fusin supplier is an individual or a company that provides Fusin active pharmaceutical ingredient (API) or Fusin finished formulations upon request. The Fusin suppliers may include Fusin API manufacturers, exporters, distributors and traders.
click here to find a list of Fusin 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 Fusin Drug Master File in Japan (Fusin JDMF) empowers Fusin 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 Fusin JDMF during the approval evaluation for pharmaceutical products. At the time of Fusin 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 Fusin suppliers with JDMF on PharmaCompass.
