01 1Life Technologies Corporation
01 1Medium / medium additive · Polyamine Supplement
01 1India
Culture medium/Culture additives Polyamine Supplement
Registration Number : 226MF40013
Registrant's Address : 3175 Staley Road Grand Island, New York 14072-0068
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-09-01
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PharmaCompass offers a list of Polyamine T 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 Polyamine T manufacturer or Polyamine T supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Polyamine T manufacturer or Polyamine T supplier.
PharmaCompass also assists you with knowing the Polyamine T API Price utilized in the formulation of products. Polyamine T API Price is not always fixed or binding as the Polyamine T Price is obtained through a variety of data sources. The Polyamine T Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Polyamine T manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polyamine T, including repackagers and relabelers. The FDA regulates Polyamine T manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polyamine T 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 Polyamine T supplier is an individual or a company that provides Polyamine T active pharmaceutical ingredient (API) or Polyamine T finished formulations upon request. The Polyamine T suppliers may include Polyamine T API manufacturers, exporters, distributors and traders.
click here to find a list of Polyamine T 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 Polyamine T Drug Master File in Japan (Polyamine T JDMF) empowers Polyamine T 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 Polyamine T JDMF during the approval evaluation for pharmaceutical products. At the time of Polyamine T 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 Polyamine T suppliers with JDMF on PharmaCompass.
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