01 1M/s MSN Laboratories
01 1Alvimopan Dihydrate IH
01 1WC-0383A4
01 1India
Date of Issue : 2019-10-15
Valid Till : 2022-08-08
Written Confirmation Number : WC-0383A4
Address of the Firm : Sy. No.455/A, 455/AA, 455/E & 455/EE Chandampet Village Shankarampet Mandal Meda...
A Alvimopan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alvimopan, including repackagers and relabelers. The FDA regulates Alvimopan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alvimopan 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 Alvimopan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alvimopan supplier is an individual or a company that provides Alvimopan active pharmaceutical ingredient (API) or Alvimopan finished formulations upon request. The Alvimopan suppliers may include Alvimopan API manufacturers, exporters, distributors and traders.
click here to find a list of Alvimopan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alvimopan written confirmation (Alvimopan WC) is an official document issued by a regulatory agency to a Alvimopan manufacturer, verifying that the manufacturing facility of a Alvimopan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Alvimopan APIs or Alvimopan finished pharmaceutical products to another nation, regulatory agencies frequently require a Alvimopan WC (written confirmation) as part of the regulatory process.
click here to find a list of Alvimopan suppliers with Written Confirmation (WC) on PharmaCompass.
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