01 1Procos S. p. A.
01 1Clofedanol Hydrochloride
01 1Italy
Registration Number : 217MF11129
Registrant's Address : Via Matteotti 249,28062 CAMERI (NOVARA)/ITALY
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2009-10-19
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PharmaCompass offers a list of Clofedanol 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 Clofedanol manufacturer or Clofedanol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clofedanol manufacturer or Clofedanol supplier.
PharmaCompass also assists you with knowing the Clofedanol API Price utilized in the formulation of products. Clofedanol API Price is not always fixed or binding as the Clofedanol Price is obtained through a variety of data sources. The Clofedanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Detigon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Detigon, including repackagers and relabelers. The FDA regulates Detigon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Detigon 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 Detigon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Detigon supplier is an individual or a company that provides Detigon active pharmaceutical ingredient (API) or Detigon finished formulations upon request. The Detigon suppliers may include Detigon API manufacturers, exporters, distributors and traders.
click here to find a list of Detigon 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 Detigon Drug Master File in Japan (Detigon JDMF) empowers Detigon 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 Detigon JDMF during the approval evaluation for pharmaceutical products. At the time of Detigon 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 Detigon suppliers with JDMF on PharmaCompass.
