01 1Osaka Synthetic Organic Chemistry Research Institute Co., Ltd.
01 1Japanese Pharmacopoeia Tosufloxacin Tosilate Hydrate Production Only
01 1Japan
Japanese Pharmacopoeia Tosufloxacin Tosylate Hydrate (For Manufacturing Use Only)
Registration Number : 303MF10097
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2021-06-22
Latest Date of Registration : 2021-06-22
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PharmaCompass offers a list of Tosufloxacin Tosylate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tosufloxacin Tosylate manufacturer or Tosufloxacin Tosylate supplier for your needs.
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A tosufloxacin tosilate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of tosufloxacin tosilate, including repackagers and relabelers. The FDA regulates tosufloxacin tosilate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. tosufloxacin tosilate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of tosufloxacin tosilate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A tosufloxacin tosilate supplier is an individual or a company that provides tosufloxacin tosilate active pharmaceutical ingredient (API) or tosufloxacin tosilate finished formulations upon request. The tosufloxacin tosilate suppliers may include tosufloxacin tosilate API manufacturers, exporters, distributors and traders.
click here to find a list of tosufloxacin tosilate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 tosufloxacin tosilate Drug Master File in Japan (tosufloxacin tosilate JDMF) empowers tosufloxacin tosilate 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 tosufloxacin tosilate JDMF during the approval evaluation for pharmaceutical products. At the time of tosufloxacin tosilate 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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