Rob Lally

Rob Lally has over 20 years of experience as a Global Regulatory Affairs leader and is an experienced negotiator with medical device regulatory agencies. Rob was most recently with Terumo Aortic where he was responsible for the US and Glasgow Regulatory Affairs teams. Previously, Rob worked for Stryker’s Joint Replacement Division where he managed a team of over 40 regulatory professionals operating in multiple US and EMEA sites. They delivered pre-approval device strategies and maintained post-approval regulatory compliance. Prior to that, Rob held various Regulatory Affairs and Quality leadership positions with BTG International, Celonova Biosciences, Smith’s medical, Staar Surgical and Johnson & Johnson. He has a BS in Mechanical Engineering and a MBA from the University of Manchester (UK).