Trey Putnam

VP, Regulatory Affairs & CMC at Fast Biomedical

As Vice President of Regulatory Affairs and CMC, Dr. Putnam oversees the development and execution of FAST BioMedical's regulatory strategy, injectable manufacturing, and quality systems. Dr. Putnam is an expert in regulatory affairs and manufacturing with Over eighteen years of product development experience. Dr. Putnam earned his Regulatory Affairs Certification (United States) in 2007 from the Regulatory Affairs Professional Society (RAPS) and is a routine contributor to the RAPS' publication Fundamentals of US Regulatory Affairs. Dr. Putnam was previously the General Manager of Cardinal Health Regulatory Sciences where he led Cardinal Health's scientific and regulatory consulting business unit which included more than 200+ regulatory affairs associates. As part of Cardinal Health Regulatory Sciences, Dr. Putnam played an integral role in the development and approval of dozens of pharmaceutical, biologic and medical device products. Dr. Putnam earned a Ph.D. and MA in Organic Chemistry from Washington University in St. Louis where his research focused on drug discovery of therapeutic oligonucleotides.

Timeline

  • VP, Regulatory Affairs & CMC

    Current role

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