01 1Esteve Quimica, S. A.
01 1Riluzole
01 1Spain
Registration Number : 224MF10021
Registrant's Address : Torre Esteve, Pg. de la Zona Franca, 109, 4th floor, 08038 Barcelona - Spain
Initial Date of Registration : 2012-02-01
Latest Date of Registration : 2012-02-01
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PharmaCompass offers a list of Riluzole 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 Riluzole manufacturer or Riluzole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Riluzole manufacturer or Riluzole supplier.
PharmaCompass also assists you with knowing the Riluzole API Price utilized in the formulation of products. Riluzole API Price is not always fixed or binding as the Riluzole Price is obtained through a variety of data sources. The Riluzole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Riluzolum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Riluzolum, including repackagers and relabelers. The FDA regulates Riluzolum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Riluzolum 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 Riluzolum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Riluzolum supplier is an individual or a company that provides Riluzolum active pharmaceutical ingredient (API) or Riluzolum finished formulations upon request. The Riluzolum suppliers may include Riluzolum API manufacturers, exporters, distributors and traders.
click here to find a list of Riluzolum 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 Riluzolum Drug Master File in Japan (Riluzolum JDMF) empowers Riluzolum 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 Riluzolum JDMF during the approval evaluation for pharmaceutical products. At the time of Riluzolum 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 Riluzolum suppliers with JDMF on PharmaCompass.
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