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This book focuses on the challenges and potentials of open source and collaborative design approaches and strategies in the biomedical field. It provides a comprehensive set of good practices and methods for making these safe, innovative and certifiable biomedical devices reach patients and provide successful solutions to healthcare issues. The chapters are sequenced to follow the complete lifecycle of open source medical technologies. The information provided is eminently practical, as it is supported by real cases of study, in which collaboration among medical professionals, engineers and technicians, patients and patient associations, policy makers, regulatory bodies, and citizens has proven beneficial. The book is also supported by an online infrastructure, UBORA, through which open-source medical devices can be collaboratively developed and shared for the democratization of medical technology and for promoting accessible biomedical engineering education.
Follows an eminently practical approach supported by several cases of success from real medical device development projects, in which collaborative design approaches and open-source strategies play a fundamental role Detailed attention is paid to all the stages of the lifecycle of open source medical devices, from the specification and conceptual stages, through the design and prototyping, towards final commercialization, production and supply chain management Provides thorough coverage of the experiences of a multidisciplinary team of experienced engineers, supported by medical professionals and key stakeholders from a wide variety of sectors, from regulators and quality supervisors, to experts in intellectual property, law and policy making
Auteur
Arti Ahluwalia, PhD, is Professor of Bioengineering at the University of Pisa (Italy). She has over 100 publications in the field of medical devices, biosensing, biomaterials, bioreactors, cell imaging and biomimetics and 15 patents, 5 of which have been industrialised. She has pioneered Open Education in BME in Africa (she was the coordinator of the UBORA project) and is a Scientific and Education Consultant for United Nation Economic Commission for Africa.Carmelo De Maria, PhD, is Assistant Professor of Bioengineering at the University of Pisa. His research interests are in the field of additive manufacturing technologies, with a particular focus in Biomedical applications, including Bioprinting and the prototyping of Medical Devices. He has several papers published in international scientific journals (over 70) and in 2016 he was awarded 1st prize as Young Investigator from the International Society for Biofabrication.
Andrés Díaz Lantada, PhD, is Professor of Mechanical Engineering at the Universidad Politecnica de Madrid. His research interests are linked to the development of mechanical systems and biomedical devices with improved capabilities, thanks to the incorporation of smart materials, special geometries and complex functional structures, attainable by additive manufacturing processes. He received the "Medal to Researchers under 40" by the Spanish Royal Academy of Engineering in 2015 and the "UPM Award to Educational Innovation Groups", as coordinator, in 2020. He is co-author of 75+ publications in international journals and author of 3 books on medical technologies.
All three Editors have been fostering the emergent field of safe open-source medical devices through the UBORA e-platform, for innovating the biomedical industry through education.
Contenu
I. FUNDAMENTALS.- 1. The medical industry: Present situation, global health concerns and outlook.- 2. General considerations for engineering open-source medical devices.-3. Systematic assessment of needs and viability analyses.-II. DESIGN METHODS FOR OPEN-SOURCE MEDICAL DEVICES.- 4. Creativity promotion: Collaborative design environments & open-innovation.-5. Safety-guided design methods for open-source medical devices.- 6. Design and simulation of open-source medical devices.- III. MANUFACTURING METHODS FOR OPEN-SOURCE MEDICAL DEVICES.- 7. Prototyping of open-source medical devices.- 8. Manufacturing of personalized open-source medical devices.- 9. Mass-production of open-source medical devices.- IV. MAKING A REAL IMPACT WITH OPEN-SOURCE MEDICAL DEVICES.- 10. Open-source medical device approval and certification.- 11. Marketing open-source medical devices: Managing quality and supply chain.- 12. Issues linked to the long-term sustainability of open-source medical devices.