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 Hydrolysine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrolysine, including repackagers and relabelers. The FDA regulates Hydrolysine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrolysine 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 Hydrolysine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrolysine supplier is an individual or a company that provides Hydrolysine active pharmaceutical ingredient (API) or Hydrolysine finished formulations upon request. The Hydrolysine suppliers may include Hydrolysine API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrolysine 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 Hydrolysine Drug Master File in Japan (Hydrolysine JDMF) empowers Hydrolysine 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 Hydrolysine JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrolysine 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 Hydrolysine suppliers with JDMF on PharmaCompass.
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