As a Principal Consultant, Danielle is an expert in leading and managing regulatory affairs projects. This includes managing regulatory affairs teams in multiple classes of trade through the completion of submissions, change control, business development activities, and maintaining global regulatory compliance.
Danielle has also spearheaded a transition of an acquisition-related manufacturer to change all global product registrations, as well as chaired the operations-based team through the implementation of corresponding rebranding activities.
Prior to MRC Global, Danielle was a Regulatory Affairs Manager at Medtronic where she managed regulatory teams and large-scale projects. Prior to Medtronic, Danielle was a Regulatory Affairs Project Manager at two medical device manufacturers – MicroPort Orthopedics and Wright Medical Technology.
Danielle received a Bachelor of Science in Physics from Rhodes College. In addition, she completed a Master of Science in Biomedical Engineering at the University of Memphis & University of Tennessee Health Science Center.