Dr. Lisa Bellincampi is an Affiliate Consultant with CardioMed Device Consultants, bringing about 20 years of experience in research and development and clinical research in the medical device industry. She helps manufacturers plan, run, and document clinical studies for medical devices and combination products, with particular depth in orthopaedics, spine, and biomaterials.
Experience
Dr. Bellincampi spent much of her career at Orthovita, a biomaterials company, where she directed R&D programs and preclinical testing to support regulatory submissions and educational programs. She went on to develop and manage post-market clinical studies in spine fusion and later served as Vice President of Clinical Research, overseeing post-market and IDE clinical programs for bone fusion, vertebroplasty, kyphoplasty, and bone screw fixation.
At Spine Wave, Inc., she oversaw IDE and post-market clinical programs for the company’s injectable disc nucleus platform and other spine applications, including global clinical trials in Europe and Australia. Her experience also includes regulatory submissions, regulatory and clinical compliance, FDA audits, and Good Clinical Practice (GCP).
At CardioMed, Dr. Bellincampi supports the planning, development, and execution of clinical trials; clinical reports and other documentation for regulatory submissions; clinical evaluation reports for CE Mark products; and medical writing, including abstracts, manuscripts, and scientific and educational presentations.