01 1Pharmacostech CO. ,LTD
01 1Tosylate tosufloxacin
01 1South Korea
Registration Number : 220MF10176
Registrant's Address : 47, Jeyakdanji-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Republic of Korea
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2008-07-31
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PharmaCompass offers a list of Tosuxacin 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 Tosuxacin manufacturer or Tosuxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tosuxacin manufacturer or Tosuxacin supplier.
PharmaCompass also assists you with knowing the Tosuxacin API Price utilized in the formulation of products. Tosuxacin API Price is not always fixed or binding as the Tosuxacin Price is obtained through a variety of data sources. The Tosuxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tosuxacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tosuxacin, including repackagers and relabelers. The FDA regulates Tosuxacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tosuxacin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tosuxacin supplier is an individual or a company that provides Tosuxacin active pharmaceutical ingredient (API) or Tosuxacin finished formulations upon request. The Tosuxacin suppliers may include Tosuxacin API manufacturers, exporters, distributors and traders.
click here to find a list of Tosuxacin 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 Tosuxacin Drug Master File in Japan (Tosuxacin JDMF) empowers Tosuxacin 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 Tosuxacin JDMF during the approval evaluation for pharmaceutical products. At the time of Tosuxacin 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 Tosuxacin suppliers with JDMF on PharmaCompass.
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