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
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PharmaCompass offers a list of Triamcinolone 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 Triamcinolone manufacturer or Triamcinolone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triamcinolone manufacturer or Triamcinolone supplier.
PharmaCompass also assists you with knowing the Triamcinolone API Price utilized in the formulation of products. Triamcinolone API Price is not always fixed or binding as the Triamcinolone Price is obtained through a variety of data sources. The Triamcinolone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-2370 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-2370, including repackagers and relabelers. The FDA regulates CS-2370 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-2370 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 CS-2370 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-2370 supplier is an individual or a company that provides CS-2370 active pharmaceutical ingredient (API) or CS-2370 finished formulations upon request. The CS-2370 suppliers may include CS-2370 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-2370 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 CS-2370 Drug Master File in Japan (CS-2370 JDMF) empowers CS-2370 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 CS-2370 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-2370 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 CS-2370 suppliers with JDMF on PharmaCompass.
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