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PharmaCompass offers a list of Gatifloxacin 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 Gatifloxacin manufacturer or Gatifloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gatifloxacin manufacturer or Gatifloxacin supplier.
PharmaCompass also assists you with knowing the Gatifloxacin API Price utilized in the formulation of products. Gatifloxacin API Price is not always fixed or binding as the Gatifloxacin Price is obtained through a variety of data sources. The Gatifloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM 1155 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM 1155, including repackagers and relabelers. The FDA regulates AM 1155 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM 1155 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 AM 1155 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM 1155 supplier is an individual or a company that provides AM 1155 active pharmaceutical ingredient (API) or AM 1155 finished formulations upon request. The AM 1155 suppliers may include AM 1155 API manufacturers, exporters, distributors and traders.
click here to find a list of AM 1155 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 AM 1155 Drug Master File in Japan (AM 1155 JDMF) empowers AM 1155 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 AM 1155 JDMF during the approval evaluation for pharmaceutical products. At the time of AM 1155 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 AM 1155 suppliers with JDMF on PharmaCompass.
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