01 1M/s MSN Laboratories
01 1Cangrelor Tetrasodium 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 Cangrelor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cangrelor, including repackagers and relabelers. The FDA regulates Cangrelor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cangrelor 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 Cangrelor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cangrelor supplier is an individual or a company that provides Cangrelor active pharmaceutical ingredient (API) or Cangrelor finished formulations upon request. The Cangrelor suppliers may include Cangrelor API manufacturers, exporters, distributors and traders.
click here to find a list of Cangrelor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cangrelor written confirmation (Cangrelor WC) is an official document issued by a regulatory agency to a Cangrelor manufacturer, verifying that the manufacturing facility of a Cangrelor active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cangrelor APIs or Cangrelor finished pharmaceutical products to another nation, regulatory agencies frequently require a Cangrelor WC (written confirmation) as part of the regulatory process.
click here to find a list of Cangrelor suppliers with Written Confirmation (WC) on PharmaCompass.
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