01 1ERREGIERRE S. p. A.
01 1Nitrate oxiconazole
01 1Italy
Registration Number : 220MF10204
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2008-09-29
Latest Date of Registration : 2008-09-29
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PharmaCompass offers a list of Oxiconazole Nitrate 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 Oxiconazole Nitrate manufacturer or Oxiconazole Nitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Oxiconazole Nitrate API Price utilized in the formulation of products. Oxiconazole Nitrate API Price is not always fixed or binding as the Oxiconazole Nitrate Price is obtained through a variety of data sources. The Oxiconazole Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fonx manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fonx, including repackagers and relabelers. The FDA regulates Fonx manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fonx 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 Fonx manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fonx supplier is an individual or a company that provides Fonx active pharmaceutical ingredient (API) or Fonx finished formulations upon request. The Fonx suppliers may include Fonx API manufacturers, exporters, distributors and traders.
click here to find a list of Fonx 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 Fonx Drug Master File in Japan (Fonx JDMF) empowers Fonx 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 Fonx JDMF during the approval evaluation for pharmaceutical products. At the time of Fonx 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 Fonx suppliers with JDMF on PharmaCompass.
