Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Flurandrenolide
01 1Germany
Axplora- The partner of choice for complex APIs.
Registration Number : 220MF10142
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2008-06-10
Latest Date of Registration : 2008-06-10
A Flurandrenolide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flurandrenolide, including repackagers and relabelers. The FDA regulates Flurandrenolide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flurandrenolide 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 Flurandrenolide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flurandrenolide supplier is an individual or a company that provides Flurandrenolide active pharmaceutical ingredient (API) or Flurandrenolide finished formulations upon request. The Flurandrenolide suppliers may include Flurandrenolide API manufacturers, exporters, distributors and traders.
click here to find a list of Flurandrenolide 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 Flurandrenolide Drug Master File in Japan (Flurandrenolide JDMF) empowers Flurandrenolide 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 Flurandrenolide JDMF during the approval evaluation for pharmaceutical products. At the time of Flurandrenolide 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 Flurandrenolide suppliers with JDMF on PharmaCompass.
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