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.
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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 WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW, including repackagers and relabelers. The FDA regulates WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW supplier is an individual or a company that provides WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW active pharmaceutical ingredient (API) or WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW finished formulations upon request. The WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW suppliers may include WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW API manufacturers, exporters, distributors and traders.
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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 WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW Drug Master File in Japan (WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW JDMF) empowers WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW 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 WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW JDMF during the approval evaluation for pharmaceutical products. At the time of WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 1 companies offering WLN: T56 BM DN FN HNJ IS- ET5N CNJ A1 DNW
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