01 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Triamcinolone "Teva"
01 1Italy
Registration Number : 218MF10983
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
A Triamcinolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamcinolone, including repackagers and relabelers. The FDA regulates Triamcinolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamcinolone 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 Triamcinolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triamcinolone supplier is an individual or a company that provides Triamcinolone active pharmaceutical ingredient (API) or Triamcinolone finished formulations upon request. The Triamcinolone suppliers may include Triamcinolone API manufacturers, exporters, distributors and traders.
click here to find a list of Triamcinolone 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 Triamcinolone Drug Master File in Japan (Triamcinolone JDMF) empowers Triamcinolone 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 Triamcinolone JDMF during the approval evaluation for pharmaceutical products. At the time of Triamcinolone 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 Triamcinolone suppliers with JDMF on PharmaCompass.
We have 1 companies offering Triamcinolone
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
