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
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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 INV-102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INV-102, including repackagers and relabelers. The FDA regulates INV-102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INV-102 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 INV-102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A INV-102 supplier is an individual or a company that provides INV-102 active pharmaceutical ingredient (API) or INV-102 finished formulations upon request. The INV-102 suppliers may include INV-102 API manufacturers, exporters, distributors and traders.
click here to find a list of INV-102 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 INV-102 Drug Master File in Japan (INV-102 JDMF) empowers INV-102 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 INV-102 JDMF during the approval evaluation for pharmaceutical products. At the time of INV-102 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 INV-102 suppliers with JDMF on PharmaCompass.
