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Sean Gemmill
Director, Regulatory Affairs, Quality

Sean Gemmill serves as the Director of Regulatory Affairs for NeoGenomics’ Pharma Services division. He joined NeoGenomics in 2018 and has been working in the field of in-vitro diagnostics and medical device clinical & regulatory affairs for over 20 years. Mr. Gemmill provides regulatory affairs support for NeoGenomics companion diagnostic (CDx) programs and US-FDA submissions. He completed his BS degree in Health Sciences (1998) and a MS degree in Biomedical & Pharmaceutical Regulatory Affairs (2003), both from San Diego State University (San Diego, CA).