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.
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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 NW 1015 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NW 1015, including repackagers and relabelers. The FDA regulates NW 1015 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NW 1015 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 NW 1015 supplier is an individual or a company that provides NW 1015 active pharmaceutical ingredient (API) or NW 1015 finished formulations upon request. The NW 1015 suppliers may include NW 1015 API manufacturers, exporters, distributors and traders.
click here to find a list of NW 1015 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 NW 1015 Drug Master File in Japan (NW 1015 JDMF) empowers NW 1015 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 NW 1015 JDMF during the approval evaluation for pharmaceutical products. At the time of NW 1015 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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