01 1Fushimi Pharmaceutical Co., Ltd.
01 1Homo sulfamine (for manufacturing only)
01 1Japan
Homosulfamine (for manufacturing only)
Registration Number : 231MF10085
Registrant's Address : 1676 Nakatsucho, Marugame City, Kagawa Prefecture
Initial Date of Registration : 2019-04-09
Latest Date of Registration : 2019-04-09
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PharmaCompass offers a list of Sulfanilamide 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 Sulfanilamide manufacturer or Sulfanilamide supplier for your needs.
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A Azol Polvo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azol Polvo, including repackagers and relabelers. The FDA regulates Azol Polvo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azol Polvo 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 Azol Polvo supplier is an individual or a company that provides Azol Polvo active pharmaceutical ingredient (API) or Azol Polvo finished formulations upon request. The Azol Polvo suppliers may include Azol Polvo 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 Azol Polvo Drug Master File in Japan (Azol Polvo JDMF) empowers Azol Polvo 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 Azol Polvo JDMF during the approval evaluation for pharmaceutical products. At the time of Azol Polvo 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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