Kimberly (Kim) Belsky is a regulatory professional with expertise in Regulatory Policy & Intelligence and AdPromo. With over 30 years of global experience in the medical product industry, including 20+ years in regulatory affairs, Kim's diverse experience including scale up and tech transfer, quality/compliance, advertising & promotion, labeling, and regulatory policy and intelligence. Her background includes Rx drug/biologics, OTCs/Nutritionals/Cosmetics, and medical devices. Kim is the co-chair of the DIA AdPromo WG (part of the RegAffairs Community) and is an active member in RAPS. Kim is passionate about networking, learning, and 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.