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The document discusses the need for medical product suppliers to conduct deep due diligence when assessing new products to address the evolving U.S. healthcare system's focus on comparative effectiveness. This means new products must prove they are at least as clinically effective as existing options and more economically effective through reduced costs. Suppliers will need to answer questions about clinical outcomes, economic impacts, and influence on reimbursement policies with compelling data. While "me too" products can easily prove parity, "innovative" products promising better outcomes will require rigorous studies. The document outlines steps and resources needed to properly evaluate new products under these new healthcare realities.









