01 1ERREGIERRE S. p. A.
01 1Bifonazole (production only)
01 1Italy
Bifonazole (for manufacturing purposes 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.
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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 Inkeysa brand of bifonazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Inkeysa brand of bifonazole, including repackagers and relabelers. The FDA regulates Inkeysa brand of bifonazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Inkeysa brand of bifonazole 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 Inkeysa brand of bifonazole supplier is an individual or a company that provides Inkeysa brand of bifonazole active pharmaceutical ingredient (API) or Inkeysa brand of bifonazole finished formulations upon request. The Inkeysa brand of bifonazole suppliers may include Inkeysa brand of bifonazole API manufacturers, exporters, distributors and traders.
click here to find a list of Inkeysa brand of bifonazole 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 Inkeysa brand of bifonazole Drug Master File in Japan (Inkeysa brand of bifonazole JDMF) empowers Inkeysa brand of bifonazole 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 Inkeysa brand of bifonazole JDMF during the approval evaluation for pharmaceutical products. At the time of Inkeysa brand of bifonazole 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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