01 1Cambrex Profarmaco Milano S. r. l.
01 1Medazepam
01 1U.S.A
Registration Number : 219MF10284
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2016-03-02
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PharmaCompass offers a list of Medazepam 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 Medazepam manufacturer or Medazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Medazepam manufacturer or Medazepam supplier.
PharmaCompass also assists you with knowing the Medazepam API Price utilized in the formulation of products. Medazepam API Price is not always fixed or binding as the Medazepam Price is obtained through a variety of data sources. The Medazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rudotel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rudotel, including repackagers and relabelers. The FDA regulates Rudotel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rudotel 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 Rudotel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rudotel supplier is an individual or a company that provides Rudotel active pharmaceutical ingredient (API) or Rudotel finished formulations upon request. The Rudotel suppliers may include Rudotel API manufacturers, exporters, distributors and traders.
click here to find a list of Rudotel 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 Rudotel Drug Master File in Japan (Rudotel JDMF) empowers Rudotel 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 Rudotel JDMF during the approval evaluation for pharmaceutical products. At the time of Rudotel 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 Rudotel suppliers with JDMF on PharmaCompass.
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