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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 0013CD6B-1671-4369-B1BE-F531611E50C7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0013CD6B-1671-4369-B1BE-F531611E50C7, including repackagers and relabelers. The FDA regulates 0013CD6B-1671-4369-B1BE-F531611E50C7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0013CD6B-1671-4369-B1BE-F531611E50C7 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 0013CD6B-1671-4369-B1BE-F531611E50C7 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0013CD6B-1671-4369-B1BE-F531611E50C7 supplier is an individual or a company that provides 0013CD6B-1671-4369-B1BE-F531611E50C7 active pharmaceutical ingredient (API) or 0013CD6B-1671-4369-B1BE-F531611E50C7 finished formulations upon request. The 0013CD6B-1671-4369-B1BE-F531611E50C7 suppliers may include 0013CD6B-1671-4369-B1BE-F531611E50C7 API manufacturers, exporters, distributors and traders.
click here to find a list of 0013CD6B-1671-4369-B1BE-F531611E50C7 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 0013CD6B-1671-4369-B1BE-F531611E50C7 Drug Master File in Japan (0013CD6B-1671-4369-B1BE-F531611E50C7 JDMF) empowers 0013CD6B-1671-4369-B1BE-F531611E50C7 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 0013CD6B-1671-4369-B1BE-F531611E50C7 JDMF during the approval evaluation for pharmaceutical products. At the time of 0013CD6B-1671-4369-B1BE-F531611E50C7 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 0013CD6B-1671-4369-B1BE-F531611E50C7 suppliers with JDMF on PharmaCompass.
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