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PharmaCompass offers a list of Lysine Acetate 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 Acetate manufacturer or Lysine Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lysine Acetate manufacturer or Lysine Acetate supplier.
PharmaCompass also assists you with knowing the Lysine Acetate API Price utilized in the formulation of products. Lysine Acetate API Price is not always fixed or binding as the Lysine Acetate Price is obtained through a variety of data sources. The Lysine Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lysine Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysine Acetate, including repackagers and relabelers. The FDA regulates Lysine Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysine Acetate 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 Lysine Acetate supplier is an individual or a company that provides Lysine Acetate active pharmaceutical ingredient (API) or Lysine Acetate finished formulations upon request. The Lysine Acetate suppliers may include Lysine Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Lysine Acetate 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 Acetate Drug Master File in Japan (Lysine Acetate JDMF) empowers Lysine Acetate 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 Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Lysine Acetate 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 Acetate suppliers with JDMF on PharmaCompass.
We have 3 companies offering Lysine Acetate
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