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