Medical Device Development Immersion is a two-day interactive course is designed for those who need to better understand the business and regulatory considerations of medical device development. The course highlights include the different regulatory pathways devices undertake for FDA or EMA marketing approval; the changing regulatory environment; a detailed explanation of the five development phases—market opportunity, evaluation, design, verification, and manufacturing; and commercialization strategies, including those for reimbursement. Learn from an industry expert with 30-years of experience in both large and start-up medical device companies.