01 1Merck KGaA
01 1Saffinamide mesylate
01 1Germany
Registration Number : 230MF10101
Registrant's Address : Frankfurter Strasse 250 64293 Darmstadt Germany
Initial Date of Registration : 2018-08-02
Latest Date of Registration : 2018-08-02
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PharmaCompass offers a list of Safinamide Methanesulfonate 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 Safinamide Methanesulfonate manufacturer or Safinamide Methanesulfonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Safinamide Methanesulfonate manufacturer or Safinamide Methanesulfonate supplier.
PharmaCompass also assists you with knowing the Safinamide Methanesulfonate API Price utilized in the formulation of products. Safinamide Methanesulfonate API Price is not always fixed or binding as the Safinamide Methanesulfonate Price is obtained through a variety of data sources. The Safinamide Methanesulfonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Safinamide Methanesulfonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Safinamide Methanesulfonate, including repackagers and relabelers. The FDA regulates Safinamide Methanesulfonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Safinamide Methanesulfonate 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 Safinamide Methanesulfonate supplier is an individual or a company that provides Safinamide Methanesulfonate active pharmaceutical ingredient (API) or Safinamide Methanesulfonate finished formulations upon request. The Safinamide Methanesulfonate suppliers may include Safinamide Methanesulfonate API manufacturers, exporters, distributors and traders.
click here to find a list of Safinamide Methanesulfonate 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 Safinamide Methanesulfonate Drug Master File in Japan (Safinamide Methanesulfonate JDMF) empowers Safinamide Methanesulfonate 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 Safinamide Methanesulfonate JDMF during the approval evaluation for pharmaceutical products. At the time of Safinamide Methanesulfonate 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 Safinamide Methanesulfonate suppliers with JDMF on PharmaCompass.
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