01 1Taenaka Mining Co., Ltd.
01 1Outsiders regulations sulfite lysine (production only)
01 1Japan
Non-regulated Lysine Sulfite (for manufacturing only)
Registration Number : 217MF10287
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2007-07-26
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PharmaCompass offers a list of Lysine 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 Lysine manufacturer or Lysine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lysine manufacturer or Lysine supplier.
PharmaCompass also assists you with knowing the Lysine API Price utilized in the formulation of products. Lysine API Price is not always fixed or binding as the Lysine Price is obtained through a variety of data sources. The Lysine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lysine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysine, including repackagers and relabelers. The FDA regulates Lysine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysine 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 Lysine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lysine supplier is an individual or a company that provides Lysine active pharmaceutical ingredient (API) or Lysine finished formulations upon request. The Lysine suppliers may include Lysine API manufacturers, exporters, distributors and traders.
click here to find a list of Lysine 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 Lysine Drug Master File in Japan (Lysine JDMF) empowers Lysine 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 Lysine JDMF during the approval evaluation for pharmaceutical products. At the time of Lysine 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 Lysine suppliers with JDMF on PharmaCompass.
