01 1Phospholipid GmbH
01 1Phosphatidylcholine (ethanol solution)
01 1Germany
Phosphatidylcholine (ethanol solution)
Registration Number : 229MF10002
Registrant's Address : Nattermannallee 1, D-50829 Cologne, Germany
Initial Date of Registration : 2017-01-10
Latest Date of Registration : 2017-01-10
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PharmaCompass offers a list of Phosphatidylcholines 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 Phosphatidylcholines manufacturer or Phosphatidylcholines supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phosphatidylcholines manufacturer or Phosphatidylcholines supplier.
PharmaCompass also assists you with knowing the Phosphatidylcholines API Price utilized in the formulation of products. Phosphatidylcholines API Price is not always fixed or binding as the Phosphatidylcholines Price is obtained through a variety of data sources. The Phosphatidylcholines Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A .Lecithin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of .Lecithin, including repackagers and relabelers. The FDA regulates .Lecithin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. .Lecithin 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 .Lecithin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A .Lecithin supplier is an individual or a company that provides .Lecithin active pharmaceutical ingredient (API) or .Lecithin finished formulations upon request. The .Lecithin suppliers may include .Lecithin API manufacturers, exporters, distributors and traders.
click here to find a list of .Lecithin 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 .Lecithin Drug Master File in Japan (.Lecithin JDMF) empowers .Lecithin 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 .Lecithin JDMF during the approval evaluation for pharmaceutical products. At the time of .Lecithin 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 .Lecithin suppliers with JDMF on PharmaCompass.
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