With Fermion, start the journey of your innovative API.
With Fermion, start the journey of your innovative API.
Registration Number : 219MF10302
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2007-09-18
Latest Date of Registration : 2024-11-13
85
PharmaCompass offers a list of Nadolol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nadolol manufacturer or Nadolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nadolol manufacturer or Nadolol supplier.
A Anabet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anabet, including repackagers and relabelers. The FDA regulates Anabet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anabet 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 Anabet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Anabet supplier is an individual or a company that provides Anabet active pharmaceutical ingredient (API) or Anabet finished formulations upon request. The Anabet suppliers may include Anabet API manufacturers, exporters, distributors and traders.
click here to find a list of Anabet suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Anabet Drug Master File in Japan (Anabet JDMF) empowers Anabet 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 Anabet JDMF during the approval evaluation for pharmaceutical products. At the time of Anabet 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 Anabet suppliers with JDMF on PharmaCompass.
