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, Price,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.
PharmaCompass also assists you with knowing the Nadolol API Price utilized in the formulation of products. Nadolol API Price is not always fixed or binding as the Nadolol Price is obtained through a variety of data sources. The Nadolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Solgol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solgol, including repackagers and relabelers. The FDA regulates Solgol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solgol 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 Solgol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solgol supplier is an individual or a company that provides Solgol active pharmaceutical ingredient (API) or Solgol finished formulations upon request. The Solgol suppliers may include Solgol API manufacturers, exporters, distributors and traders.
click here to find a list of Solgol 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 Solgol Drug Master File in Japan (Solgol JDMF) empowers Solgol 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 Solgol JDMF during the approval evaluation for pharmaceutical products. At the time of Solgol 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 Solgol suppliers with JDMF on PharmaCompass.
