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 Cytamid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytamid, including repackagers and relabelers. The FDA regulates Cytamid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytamid 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 Cytamid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytamid supplier is an individual or a company that provides Cytamid active pharmaceutical ingredient (API) or Cytamid finished formulations upon request. The Cytamid suppliers may include Cytamid API manufacturers, exporters, distributors and traders.
click here to find a list of Cytamid 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 Cytamid Drug Master File in Japan (Cytamid JDMF) empowers Cytamid 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 Cytamid JDMF during the approval evaluation for pharmaceutical products. At the time of Cytamid 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 Cytamid suppliers with JDMF on PharmaCompass.
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