Daniel Sheidy, PhD, is an experienced regulatory writer currently serving as Associate Director at AbbVie, where they manage a team of writers and author complex regulatory documents for various therapeutic areas. With over seven years of regulatory writing experience and twelve years in scientific research and development, Daniel has contributed significantly to clinical development in pharmaceuticals and medical devices. They earned a PhD in Molecular, Cellular, and Developmental Biology from the University of Michigan and have held various roles in esteemed institutions such as MMS Holdings and Upland Nanotech. Daniel's work has included mentoring junior writers and optimizing processes to enhance departmental efficiency.
This person is not in any teams
This person is not in any offices