Medical Device Management : A Comprehensive Guide to Markets, Marketing, and Regulations / [electronic resource] : / edited by Andreas Krämer, Cosimo Franco, Fabiola Hartung-Linz, Ellen Thom.. — 1st ed. 2026.. — XIX, 514 p. 35 illus. : online resource. — (Springer Series in Healthcare Management and Innovation,) 3091-3829. - Springer Series in Healthcare Management and Innovation, .
PART I – Medical Devices: an overview. -- 1. Introduction: Medical Devices in a VUCA world. -- 2. Relevance of Medical Devices to humans and their impact in different geographical areas. -- 3. Why is there a need for control and regulation?. -- 4. Market environment: stakeholder analysis. -- 5. Overall health strategy of the European Union. -- PART II – Medical Devices: from devices to revenue. -- 6. Categories, characteristics and developments. -- 7. Role of technology in the Medical Devices business. -- 8. Quality and Risks. -- 9. Innovation processes and “speed to market”. -- 10. Business and revenue models. -- 11. Profitability and the role of pricing. -- PART III – Medical Devices: Legal and Regulatory framework. -- 12. Direct and indirect regulations for Medical Devices. -- 13. Medical Devices certification process. -- 14. Legal implications for manufactures and other stakeholders. -- 15. A brief regulation overview in the most important geographical areas. -- PART IV – Medical Devices: Markets and market developments. -- 16. Market perspective big players (Case A). -- 17. Market perspective small players (Case B). -- 18. Market perspective new player/start-ups. -- 19. The role of platforms and networks. -- 20. Commercialization and sales. -- 21. National vs international markets and the role of developing nations. -- PART V – Outlook: the future of Medical Devices. -- 22. The role of sustainability and ESG. -- 23. Competences required by the future Medical Device market. -- 24. Outlook: future drivers of the market.
Open Access
Анотація: Medical Devices are an extremely important, versatile and complex product category within healthcare. However, compared to medicinal products, hospitals, medical staff, etc., there is much less general awareness and understanding of medical devices. This book illuminates different facets of medical devices in a holistic manner. It describes the complexity of the industry, markets, manufacturers, and numerous other stakeholders as well as related regulations, required competencies, and future trends. More specifically, it describes a range of products and innovations, safety risks and regulations, legal aspects, and certification processes. It also examines the market from the point of view of the manufacturer from start-ups to large companies and conglomerates. Finally, this book looks at the special role sustainability and ESG plays in the future of medical device innovation, production, and usage. Featuring industry case studies this book is ideal for individuals, from scientists to managers, interested in healthcare and who would like to understand the overall relevance of medical devices from different perspectives, specifically interactions, developments and dynamics between the different business areas and stakeholders. This book is open access.
9783032035776
10.1007/978-3-032-03577-6 doi
Health services administration. Biomedical engineering. Technological innovations. Practice of medicine. Hospitals--Administration. Health Care Management. Medical and Health Technologies. Innovation and Technology Management. Biomedical Devices and Instrumentation. Practice and Hospital Management.