Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Fluocinolone Acetonide
01 1Germany
Axplora- The partner of choice for complex APIs.
Registration Number : 218MF10445
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2010-03-17
A Fluocinolone Acetonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluocinolone Acetonide, including repackagers and relabelers. The FDA regulates Fluocinolone Acetonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluocinolone Acetonide 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 Fluocinolone Acetonide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluocinolone Acetonide supplier is an individual or a company that provides Fluocinolone Acetonide active pharmaceutical ingredient (API) or Fluocinolone Acetonide finished formulations upon request. The Fluocinolone Acetonide suppliers may include Fluocinolone Acetonide API manufacturers, exporters, distributors and traders.
click here to find a list of Fluocinolone Acetonide 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 Fluocinolone Acetonide Drug Master File in Japan (Fluocinolone Acetonide JDMF) empowers Fluocinolone Acetonide 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 Fluocinolone Acetonide JDMF during the approval evaluation for pharmaceutical products. At the time of Fluocinolone Acetonide 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 Fluocinolone Acetonide suppliers with JDMF on PharmaCompass.
We have 1 companies offering Fluocinolone Acetonide
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
