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 Goutnil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Goutnil, including repackagers and relabelers. The FDA regulates Goutnil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Goutnil 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 Goutnil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Goutnil supplier is an individual or a company that provides Goutnil active pharmaceutical ingredient (API) or Goutnil finished formulations upon request. The Goutnil suppliers may include Goutnil API manufacturers, exporters, distributors and traders.
click here to find a list of Goutnil 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 Goutnil Drug Master File in Japan (Goutnil JDMF) empowers Goutnil 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 Goutnil JDMF during the approval evaluation for pharmaceutical products. At the time of Goutnil 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 Goutnil suppliers with JDMF on PharmaCompass.
