01 1Corden Pharma Bergamo S. p. A.
01 1METRONIDAZOLE
01 1Italy
Registration Number : 220MF10104
Registrant's Address : Via Bergamo, 121, I-24047, TREVIGLIO (Bg), Italy
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2015-11-12
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PharmaCompass offers a list of Metronidazole 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 Metronidazole manufacturer or Metronidazole supplier for your needs.
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PharmaCompass also assists you with knowing the Metronidazole API Price utilized in the formulation of products. Metronidazole API Price is not always fixed or binding as the Metronidazole Price is obtained through a variety of data sources. The Metronidazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A metronidazole|Metronidaz manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of metronidazole|Metronidaz, including repackagers and relabelers. The FDA regulates metronidazole|Metronidaz manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. metronidazole|Metronidaz API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A metronidazole|Metronidaz supplier is an individual or a company that provides metronidazole|Metronidaz active pharmaceutical ingredient (API) or metronidazole|Metronidaz finished formulations upon request. The metronidazole|Metronidaz suppliers may include metronidazole|Metronidaz API manufacturers, exporters, distributors and traders.
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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 metronidazole|Metronidaz Drug Master File in Japan (metronidazole|Metronidaz JDMF) empowers metronidazole|Metronidaz 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 metronidazole|Metronidaz JDMF during the approval evaluation for pharmaceutical products. At the time of metronidazole|Metronidaz JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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