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 Streptocid album manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Streptocid album, including repackagers and relabelers. The FDA regulates Streptocid album manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Streptocid album 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 Streptocid album supplier is an individual or a company that provides Streptocid album active pharmaceutical ingredient (API) or Streptocid album finished formulations upon request. The Streptocid album suppliers may include Streptocid album 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 Streptocid album Drug Master File in Japan (Streptocid album JDMF) empowers Streptocid album 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 Streptocid album JDMF during the approval evaluation for pharmaceutical products. At the time of Streptocid album 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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