01 1Osaka Synthetic Organic Chemical Research Institute, Inc.
01 1Only the Japanese Pharmacopoeia ifenprodil tartrate salt production
01 1Japan
Japanese Pharmacopoeia Ifenprodil Tartrate For manufacturing only
Registration Number : 218MF10594
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
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PharmaCompass offers a list of Cerocral 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 Cerocral manufacturer or Cerocral supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cerocral manufacturer or Cerocral supplier.
PharmaCompass also assists you with knowing the Cerocral API Price utilized in the formulation of products. Cerocral API Price is not always fixed or binding as the Cerocral Price is obtained through a variety of data sources. The Cerocral Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Validex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Validex, including repackagers and relabelers. The FDA regulates Validex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Validex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Validex supplier is an individual or a company that provides Validex active pharmaceutical ingredient (API) or Validex finished formulations upon request. The Validex suppliers may include Validex API manufacturers, exporters, distributors and traders.
click here to find a list of Validex 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 Validex Drug Master File in Japan (Validex JDMF) empowers Validex 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 Validex JDMF during the approval evaluation for pharmaceutical products. At the time of Validex 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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