Sandeep Ramineni, Ph.D., leverages his extensive experience in biomaterials, drug delivery systems and regenerative medicine to excel as a Product Assessment Expert/Auditor at TÜV SÜD Inc. After conducting applied research in these fields, Dr. Ramineni transitioned to the medical device industry, where he developed orthopedic and diagnostic devices. Currently, he applies his expertise at TÜV SÜD by assessing Class III devices and conducting audits for various schemes, including ISO 13485, EU MDR and MDSAP. Dr.Ramineni’s daily frontline experience evaluating products for MDR certification grants him invaluable, up-to-date knowledge and insights into MDR nuances, interpretations and real-world applications.