01 1Hayashibara Co., Ltd.
01 1interferon-α "Hayashibara" HSA-free
01 1Japan
Interferon-α "Hayashibara" HSA-free
Registration Number : 217MF10026
Registrant's Address : Okayama City, Kita Ward, Shimoishii 1-2-3
Initial Date of Registration : 2005-05-18
Latest Date of Registration : 2006-04-07
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PharmaCompass offers a list of Interferon Alfa-2B 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 Interferon Alfa-2B manufacturer or Interferon Alfa-2B supplier for your needs.
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PharmaCompass also assists you with knowing the Interferon Alfa-2B API Price utilized in the formulation of products. Interferon Alfa-2B API Price is not always fixed or binding as the Interferon Alfa-2B Price is obtained through a variety of data sources. The Interferon Alfa-2B Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Intron A (Interferon) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Intron A (Interferon), including repackagers and relabelers. The FDA regulates Intron A (Interferon) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Intron A (Interferon) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Intron A (Interferon) supplier is an individual or a company that provides Intron A (Interferon) active pharmaceutical ingredient (API) or Intron A (Interferon) finished formulations upon request. The Intron A (Interferon) suppliers may include Intron A (Interferon) API manufacturers, exporters, distributors and traders.
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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 Intron A (Interferon) Drug Master File in Japan (Intron A (Interferon) JDMF) empowers Intron A (Interferon) 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 Intron A (Interferon) JDMF during the approval evaluation for pharmaceutical products. At the time of Intron A (Interferon) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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