01 2Life Technologies Corporation
01 1Medium / medium additive · Cholesterol Lipid Concentrate
02 1Medium / medium additive · Cholesterol Lipid Concentrate 100 0X Aqueous Liquid
01 2India
Culture medium/Culture medium additive: Cholesterol Liquid Concentrate 1000X Aqueous Liquid
Registration Number : 226MF40025
Registrant's Address : 3175 Staley Road Grand Island, New York 14072-0068
Initial Date of Registration : 2014-12-05
Latest Date of Registration : 2014-12-05
Culture medium / Culture medium additive: Cholesterol Lipid Concentrate
Registration Number : 226MF40001
Registrant's Address : 3175 Staley Road Grand Island, New York 14072-0068
Initial Date of Registration : 2014-01-27
Latest Date of Registration : 2020-07-06
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A Dusoran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dusoran, including repackagers and relabelers. The FDA regulates Dusoran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dusoran 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 Dusoran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dusoran supplier is an individual or a company that provides Dusoran active pharmaceutical ingredient (API) or Dusoran finished formulations upon request. The Dusoran suppliers may include Dusoran API manufacturers, exporters, distributors and traders.
click here to find a list of Dusoran suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Dusoran Drug Master File in Japan (Dusoran JDMF) empowers Dusoran 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 Dusoran JDMF during the approval evaluation for pharmaceutical products. At the time of Dusoran 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 Dusoran suppliers with JDMF on PharmaCompass.
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