Lee Mullin, PhD
Lee Mullin, PhD combines her scientific and regulatory background with her technical writing skills to prepare FDA advisory committee briefing documents and panel packs. Lee’s attention to detail and editing experience help her clearly explain the complex information required for credible briefing documents. Lee’s expertise in medical imaging and drug delivery, and extensive training in interdisciplinary and translational research, enables her to effectively collaborate with teams at all stages of product development. Prior to joining 3D, Lee worked as a medical device regulatory consultant. Lee is regulatory affairs certified (RAC US) by the Regulatory Affairs Professional Society and has a PhD in Biomedical Engineering.