Melissa has 22 years experience in successful planning and execution of regulatory strategies and clinical trial programs for new product development, developing quality systems, and managing Regulatory due diligence and integration of new business partners. Melissa’s focus is working with medical device, pharmaceutical, and biologic companies on product development, strategic regulatory and clinical planning, and functional gap analyses.
Before consulting independently, Melissa was a Managing Director at Halloran Consulting Group. Previously to that Melissa was the Director of Corporate Regulatory Affairs at Boston Scientific Corporation in Natick, MA. Prior to joining Boston Scientific, Melissa was the Director of Regulatory and Clinical Affairs at Interventional Therapies, as well as Vivatone Hearing Systems. Melissa also held a Regulatory Affairs position at US Surgical Corporation.
Education: Melissa is RAC certified. She holds an MS in Human Nutrition from the University of Bridgeport and a BS in Biology from Eastern Connecticut State University.