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Shawn Shirazi

Shawn Shirazi has 20+ years of hands-on experience in pharmaceutical drug formulation and development, clinical trial management, Good Manufacturing Practices (“GMP”) international drug manufacture, international regulatory guidelines and quality assurance in GMP drug manufacture. He has held senior roles with both start-ups and large pharmaceutical organizations and led the generic drug development programs for numerous pharmaceutical organizations, resulting in multiple “First To File” drug applications.

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