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Marc Constant, PharmD
Senior Director, CMC at NoNO Inc.


Marc C Constant has over 20 years of biopharmaceutical industry experience in operational positions in both Regulatory Affairs and Quality Assurance. He previously worked at UCB and Sanofi Pasteur in different CMC positions responsible for developing and leading Technology Transfer strategies, new drug product presentations, new manufacturing facilities for API and drug product, process scale up including Quality by Design, risk management, quality control strategies and comparability principles for both new drug application and mature product. In his current position at NoNO Inc., he is responsible for the CMC program and oversight of operations at both manufacturing and control sites.

Agenda Sessions

  • Case Study: Drug Substance Dual Sourcing: An Overview of the Execution of a CMC Validation Strategy including a Second Site