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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PharmaCompass offers a list of Cholesterol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Cholesterol manufacturer or Cholesterol supplier for your needs.
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A Dythol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dythol, including repackagers and relabelers. The FDA regulates Dythol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dythol 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 Dythol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Dythol supplier is an individual or a company that provides Dythol active pharmaceutical ingredient (API) or Dythol finished formulations upon request. The Dythol suppliers may include Dythol API manufacturers, exporters, distributors and traders.
click here to find a list of Dythol 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 Dythol Drug Master File in Japan (Dythol JDMF) empowers Dythol 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 Dythol JDMF during the approval evaluation for pharmaceutical products. At the time of Dythol 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 Dythol suppliers with JDMF on PharmaCompass.
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