01 1Derivados Quimicos sau
01 1Flutamide
01 1Spain
Registration Number : 217MF11174
Registrant's Address : Camino de Pliego, No. 150, Alcantarilla, 30820, Murcia, Spain
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2019-10-11
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PharmaCompass offers a list of Flutamide 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 Flutamide manufacturer or Flutamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flutamide manufacturer or Flutamide supplier.
PharmaCompass also assists you with knowing the Flutamide API Price utilized in the formulation of products. Flutamide API Price is not always fixed or binding as the Flutamide Price is obtained through a variety of data sources. The Flutamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chimax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chimax, including repackagers and relabelers. The FDA regulates Chimax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chimax 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 Chimax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chimax supplier is an individual or a company that provides Chimax active pharmaceutical ingredient (API) or Chimax finished formulations upon request. The Chimax suppliers may include Chimax API manufacturers, exporters, distributors and traders.
click here to find a list of Chimax 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 Chimax Drug Master File in Japan (Chimax JDMF) empowers Chimax 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 Chimax JDMF during the approval evaluation for pharmaceutical products. At the time of Chimax 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 Chimax suppliers with JDMF on PharmaCompass.
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