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PharmaCompass offers a list of Fluorometholone 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 Fluorometholone manufacturer or Fluorometholone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluorometholone manufacturer or Fluorometholone supplier.
PharmaCompass also assists you with knowing the Fluorometholone API Price utilized in the formulation of products. Fluorometholone API Price is not always fixed or binding as the Fluorometholone Price is obtained through a variety of data sources. The Fluorometholone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fluorometholone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluorometholone, including repackagers and relabelers. The FDA regulates Fluorometholone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluorometholone 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 Fluorometholone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluorometholone supplier is an individual or a company that provides Fluorometholone active pharmaceutical ingredient (API) or Fluorometholone finished formulations upon request. The Fluorometholone suppliers may include Fluorometholone API manufacturers, exporters, distributors and traders.
click here to find a list of Fluorometholone 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 Fluorometholone Drug Master File in Japan (Fluorometholone JDMF) empowers Fluorometholone 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 Fluorometholone JDMF during the approval evaluation for pharmaceutical products. At the time of Fluorometholone 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 Fluorometholone suppliers with JDMF on PharmaCompass.
We have 3 companies offering Fluorometholone
Get in contact with the supplier of your choice:
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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
