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