01 1Bussan Food Science Co., Ltd.
01 1Japanese Pharmacopoeia D- mannitol
01 1Japan
Japanese Pharmacopoeia D-Mannitol
Registration Number : 218MF10311
Registrant's Address : 24-12 Kitahamacho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
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PharmaCompass offers a list of Mannitol API 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 Mannitol API manufacturer or Mannitol API supplier for your needs.
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A Resectisol In Plastic Container manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resectisol In Plastic Container, including repackagers and relabelers. The FDA regulates Resectisol In Plastic Container manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resectisol In Plastic Container 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 Resectisol In Plastic Container supplier is an individual or a company that provides Resectisol In Plastic Container active pharmaceutical ingredient (API) or Resectisol In Plastic Container finished formulations upon request. The Resectisol In Plastic Container suppliers may include Resectisol In Plastic Container 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 Resectisol In Plastic Container Drug Master File in Japan (Resectisol In Plastic Container JDMF) empowers Resectisol In Plastic Container 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 Resectisol In Plastic Container JDMF during the approval evaluation for pharmaceutical products. At the time of Resectisol In Plastic Container 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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