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