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 CS-2241 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-2241, including repackagers and relabelers. The FDA regulates CS-2241 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-2241 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 CS-2241 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-2241 supplier is an individual or a company that provides CS-2241 active pharmaceutical ingredient (API) or CS-2241 finished formulations upon request. The CS-2241 suppliers may include CS-2241 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-2241 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 CS-2241 Drug Master File in Japan (CS-2241 JDMF) empowers CS-2241 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 CS-2241 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-2241 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 CS-2241 suppliers with JDMF on PharmaCompass.
