01 1Alfresa Fine Chemical Co., Ltd.
01 1Pantethine
01 1Japan
Registration Number : 217MF10955
Registrant's Address : 1-10-1 Mukaihama, Akita City, Akita Prefecture
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2007-04-27
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PharmaCompass offers a list of Pantethine 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 Pantethine manufacturer or Pantethine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pantethine manufacturer or Pantethine supplier.
PharmaCompass also assists you with knowing the Pantethine API Price utilized in the formulation of products. Pantethine API Price is not always fixed or binding as the Pantethine Price is obtained through a variety of data sources. The Pantethine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Liponet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liponet, including repackagers and relabelers. The FDA regulates Liponet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liponet 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 Liponet supplier is an individual or a company that provides Liponet active pharmaceutical ingredient (API) or Liponet finished formulations upon request. The Liponet suppliers may include Liponet API manufacturers, exporters, distributors and traders.
click here to find a list of Liponet 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 Liponet Drug Master File in Japan (Liponet JDMF) empowers Liponet 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 Liponet JDMF during the approval evaluation for pharmaceutical products. At the time of Liponet 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 Liponet suppliers with JDMF on PharmaCompass.
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