Registration Number : 218MF10226
Registrant's Address : Viale Ortles 12 Milan Italy
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2022-02-17
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PharmaCompass offers a list of Colchicine 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 Colchicine manufacturer or Colchicine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Colchicine manufacturer or Colchicine supplier.
PharmaCompass also assists you with knowing the Colchicine API Price utilized in the formulation of products. Colchicine API Price is not always fixed or binding as the Colchicine Price is obtained through a variety of data sources. The Colchicine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kolkicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kolkicin, including repackagers and relabelers. The FDA regulates Kolkicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kolkicin 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 Kolkicin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Kolkicin supplier is an individual or a company that provides Kolkicin active pharmaceutical ingredient (API) or Kolkicin finished formulations upon request. The Kolkicin suppliers may include Kolkicin API manufacturers, exporters, distributors and traders.
click here to find a list of Kolkicin 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 Kolkicin Drug Master File in Japan (Kolkicin JDMF) empowers Kolkicin 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 Kolkicin JDMF during the approval evaluation for pharmaceutical products. At the time of Kolkicin 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 Kolkicin suppliers with JDMF on PharmaCompass.
