01 1M/s. Apicore Pharmaceuticals Pvt. Ltd.,
01 1Miglustat IH
01 1WC-0110n
01 1India
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0110n
Address of the Firm : 252-253, Dhobikuva-391 440, Opp.Jain Irrigation, Padra Jambusar Highway, Tal.Pad...
A Miglustat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Miglustat, including repackagers and relabelers. The FDA regulates Miglustat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Miglustat 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 Miglustat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Miglustat supplier is an individual or a company that provides Miglustat active pharmaceutical ingredient (API) or Miglustat finished formulations upon request. The Miglustat suppliers may include Miglustat API manufacturers, exporters, distributors and traders.
click here to find a list of Miglustat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Miglustat written confirmation (Miglustat WC) is an official document issued by a regulatory agency to a Miglustat manufacturer, verifying that the manufacturing facility of a Miglustat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Miglustat APIs or Miglustat finished pharmaceutical products to another nation, regulatory agencies frequently require a Miglustat WC (written confirmation) as part of the regulatory process.
click here to find a list of Miglustat suppliers with Written Confirmation (WC) on PharmaCompass.
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