01 1Osaka Synthetic Organic Chemical Research Institute, Inc.
01 1Japanese Pharmacopoeia Tosufloxacin Tosilate Hydrate Production Only
01 1Japan
Japanese Pharmacopoeia Tosufloxacin Tosilate Hydrate For manufacturing 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
A Tosufloxacin Tosylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tosufloxacin Tosylate, including repackagers and relabelers. The FDA regulates Tosufloxacin Tosylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tosufloxacin Tosylate 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 Tosylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tosufloxacin Tosylate supplier is an individual or a company that provides Tosufloxacin Tosylate active pharmaceutical ingredient (API) or Tosufloxacin Tosylate finished formulations upon request. The Tosufloxacin Tosylate suppliers may include Tosufloxacin Tosylate API manufacturers, exporters, distributors and traders.
click here to find a list of Tosufloxacin Tosylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Tosylate Drug Master File in Japan (Tosufloxacin Tosylate JDMF) empowers Tosufloxacin Tosylate 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 Tosylate JDMF during the approval evaluation for pharmaceutical products. At the time of Tosufloxacin Tosylate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Tosufloxacin Tosylate suppliers with JDMF on PharmaCompass.
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