01 1M/s. Sun Pharmaceuticals Industries Ltd.
01 1Bivalirudin (IH)
01 1WC-0159
01 1India
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159
Address of the Firm : A-7/A-8, MIDC, Ahmednagar-414 111, Maharashtra State
A Bivalirudin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bivalirudin, including repackagers and relabelers. The FDA regulates Bivalirudin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bivalirudin 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 Bivalirudin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bivalirudin supplier is an individual or a company that provides Bivalirudin active pharmaceutical ingredient (API) or Bivalirudin finished formulations upon request. The Bivalirudin suppliers may include Bivalirudin API manufacturers, exporters, distributors and traders.
click here to find a list of Bivalirudin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bivalirudin written confirmation (Bivalirudin WC) is an official document issued by a regulatory agency to a Bivalirudin manufacturer, verifying that the manufacturing facility of a Bivalirudin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bivalirudin APIs or Bivalirudin finished pharmaceutical products to another nation, regulatory agencies frequently require a Bivalirudin WC (written confirmation) as part of the regulatory process.
click here to find a list of Bivalirudin suppliers with Written Confirmation (WC) on PharmaCompass.
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