01 1Amino Chemicals Ltd.
01 1Miglustat
01 1Malta
Registration Number : 306MF10076
Registrant's Address : MRA050X, INDUSTRIAL ESTATE MARSA MRS 3000 Malta
Initial Date of Registration : 2024-06-06
Latest Date of Registration : 2024-06-06
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PharmaCompass offers a list of Miglustat 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 Miglustat manufacturer or Miglustat supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Miglustat manufacturer or Miglustat supplier.
PharmaCompass also assists you with knowing the Miglustat API Price utilized in the formulation of products. Miglustat API Price is not always fixed or binding as the Miglustat Price is obtained through a variety of data sources. The Miglustat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zavesca manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zavesca, including repackagers and relabelers. The FDA regulates Zavesca manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zavesca 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 Zavesca manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zavesca supplier is an individual or a company that provides Zavesca active pharmaceutical ingredient (API) or Zavesca finished formulations upon request. The Zavesca suppliers may include Zavesca API manufacturers, exporters, distributors and traders.
click here to find a list of Zavesca 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 Zavesca Drug Master File in Japan (Zavesca JDMF) empowers Zavesca 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 Zavesca JDMF during the approval evaluation for pharmaceutical products. At the time of Zavesca 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 Zavesca suppliers with JDMF on PharmaCompass.
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