Holly Rhodes is the Director of Orthopedic Regulatory Affairs at Musculoskeletal Clinical Regulatory Advisors (MCRA). Rhodes is a senior regulatory affairs professional with time‐tested record developing highly effective client strategies for ascertaining the most appropriate and efficient regulatory pathways for new products and for existing products with new indications and expediting FDA clearances.

Prior to her role at MCRA, Rhodes spent over 25 years a Lead Reviewer and Biomedical Engineer at where she led reviews of 400+ 510(k)s, 25 IDEs, and 10 PMAs for orthopedic and joint devices, including hips, knees, ankles, shoulders, wrists, toes, suture anchors, spinal systems, and fracture fixation systems.