Kimberly (Kim) Belsky is a seasoned regulatory professional specializing in Regulatory Policy, Intelligence, and Advertising & Promotion (AdPromo). With over 30 years of global experience in the medical product industry, including more than 20 years in regulatory affairs. Her diverse background spans prescription drugs, biologics, over-the-counter products, nutritionals, cosmetics, and medical devices. She also happily co-chairs the DIA AdPromo Working Group within the Regulatory Affairs Community and is actively involved in the Regulatory Affairs Professional Society (RAPS). Kim is passionate about networking, learning, sharing insights and fostering collaboration.

Dr. Lisa Jenkins is the VP of Regulatory Strategy and Content Development at Virtual Regulatory Solutions, a company designed to assist small companies develop, register, and maintain drug, biologic, device, and generic applications. Dr. Jenkins has 15+ years of experience in the life sciences industry, and specializes in eCTD submissions management, adaptive clinical trial design, biomarkers, product labeling, and risk management planning. Dr. Jenkins serves as the Deputy Editor of TIRS.