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 Flurandrenolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flurandrenolone, including repackagers and relabelers. The FDA regulates Flurandrenolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flurandrenolone 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 Flurandrenolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flurandrenolone supplier is an individual or a company that provides Flurandrenolone active pharmaceutical ingredient (API) or Flurandrenolone finished formulations upon request. The Flurandrenolone suppliers may include Flurandrenolone API manufacturers, exporters, distributors and traders.
click here to find a list of Flurandrenolone 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 Flurandrenolone Drug Master File in Japan (Flurandrenolone JDMF) empowers Flurandrenolone 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 Flurandrenolone JDMF during the approval evaluation for pharmaceutical products. At the time of Flurandrenolone 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 Flurandrenolone suppliers with JDMF on PharmaCompass.
We have 1 companies offering Flurandrenolone
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
