01 1Katsura Chemical Co., Ltd.
01 1Pre-di Nord mesylate
01 1Japan
Registration Number : 219MF10240
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
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PharmaCompass offers a list of Pridinol 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 Pridinol manufacturer or Pridinol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pridinol manufacturer or Pridinol supplier.
PharmaCompass also assists you with knowing the Pridinol API Price utilized in the formulation of products. Pridinol API Price is not always fixed or binding as the Pridinol Price is obtained through a variety of data sources. The Pridinol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lyseen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lyseen, including repackagers and relabelers. The FDA regulates Lyseen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lyseen 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 Lyseen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lyseen supplier is an individual or a company that provides Lyseen active pharmaceutical ingredient (API) or Lyseen finished formulations upon request. The Lyseen suppliers may include Lyseen API manufacturers, exporters, distributors and traders.
click here to find a list of Lyseen 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 Lyseen Drug Master File in Japan (Lyseen JDMF) empowers Lyseen 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 Lyseen JDMF during the approval evaluation for pharmaceutical products. At the time of Lyseen 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 Lyseen suppliers with JDMF on PharmaCompass.
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