01 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Mitomycin C
01 1Italy
Registration Number : 304MF10010
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2022-01-11
Latest Date of Registration : 2024-02-14
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PharmaCompass offers a list of Mitomycin 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 Mitomycin manufacturer or Mitomycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mitomycin manufacturer or Mitomycin supplier.
PharmaCompass also assists you with knowing the Mitomycin API Price utilized in the formulation of products. Mitomycin API Price is not always fixed or binding as the Mitomycin Price is obtained through a variety of data sources. The Mitomycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A M2320 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of M2320, including repackagers and relabelers. The FDA regulates M2320 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. M2320 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 M2320 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A M2320 supplier is an individual or a company that provides M2320 active pharmaceutical ingredient (API) or M2320 finished formulations upon request. The M2320 suppliers may include M2320 API manufacturers, exporters, distributors and traders.
click here to find a list of M2320 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 M2320 Drug Master File in Japan (M2320 JDMF) empowers M2320 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 M2320 JDMF during the approval evaluation for pharmaceutical products. At the time of M2320 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 M2320 suppliers with JDMF on PharmaCompass.
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