01 1ERREGIERRE S. p. A.
01 1Bifonazole (production only)
01 1Italy
Bifonazole (for manufacturing only)
Registration Number : 221MF10279
Registrant's Address : Via F. Baracca 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2009-12-18
Latest Date of Registration : 2009-12-18
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PharmaCompass offers a list of Bifonazole 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 Bifonazole manufacturer or Bifonazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bifonazole manufacturer or Bifonazole supplier.
PharmaCompass also assists you with knowing the Bifonazole API Price utilized in the formulation of products. Bifonazole API Price is not always fixed or binding as the Bifonazole Price is obtained through a variety of data sources. The Bifonazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bifon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bifon, including repackagers and relabelers. The FDA regulates Bifon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bifon 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 Bifon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bifon supplier is an individual or a company that provides Bifon active pharmaceutical ingredient (API) or Bifon finished formulations upon request. The Bifon suppliers may include Bifon API manufacturers, exporters, distributors and traders.
click here to find a list of Bifon 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 Bifon Drug Master File in Japan (Bifon JDMF) empowers Bifon 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 Bifon JDMF during the approval evaluation for pharmaceutical products. At the time of Bifon 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 Bifon suppliers with JDMF on PharmaCompass.
