The development and commercialization of contemporary medical devices are inherently multidisciplinary. Consequently, they have to undergo a stringent regulatory compliance procedure in conformity with an ever increasingly fierce and competitive business environment. Throughout the product life cycle, medical devices would significantly consume renewable as well as non-renewable resources and as a result exert a substantial social, economic and environmental impact(s). Sustainability from an overall perspective in terms of social, economic and environmental domains is crucial for decision-making during product development; nevertheless they have rarely been incorporated simultaneously. Both public and private institutions only focused tow...