The Innovation Law Center at the Syracuse University College of Law welcomes FDA consultant Gary Brennan to its “Ask the Innovator” session on Thursday, October 14 at noon. Brennan is an FDA medical device regulatory expert. He has worked in the Medical Device Quality and Regulatory Affairs field for over fifteen years managing many aspects of FDA regulatory compliance from product development to product lifecycle management. He will talk about commonly asked questions encountered by early-stage medical device companies. To learn more, read here.