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