With Fermion, start the journey of your innovative API.
With Fermion, start the journey of your innovative API.
Registration Number : 219MF10383
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2007-12-19
Latest Date of Registration : 2018-11-16
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PharmaCompass offers a list of Azathioprine 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 Azathioprine manufacturer or Azathioprine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azathioprine manufacturer or Azathioprine supplier.
PharmaCompass also assists you with knowing the Azathioprine API Price utilized in the formulation of products. Azathioprine API Price is not always fixed or binding as the Azathioprine Price is obtained through a variety of data sources. The Azathioprine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Muran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Muran, including repackagers and relabelers. The FDA regulates Muran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Muran 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 Muran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Muran supplier is an individual or a company that provides Muran active pharmaceutical ingredient (API) or Muran finished formulations upon request. The Muran suppliers may include Muran API manufacturers, exporters, distributors and traders.
click here to find a list of Muran 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 Muran Drug Master File in Japan (Muran JDMF) empowers Muran 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 Muran JDMF during the approval evaluation for pharmaceutical products. At the time of Muran 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 Muran suppliers with JDMF on PharmaCompass.
