Contents
Part IConcepts, Tools, Processes
Section IBTools, Processes and Actors
12Participatory Governance in Health Research: Patients and Publics as Stewards of Health Research Systems
14The Regulatory Role of Patents in Innovative Health Research and Its Translation from the Laboratory to the Clinic
16Taking Failure Seriously: Health Research Regulation for Medical Devices, Technological Risk and Preventing Future Harm
17Rules, Principles and the Added Value of Best Practice in Health Research Regulation
20Is the Red Queen Sitting on the Throne? Current Trends and Future Developments in Human Health Research Regulation
21Regulatory Authorities and Decision-Making in Health Research: The Institutional Dimension
22The Once and Future Role of Policy Advice for Health Regulation by Experts and Advisory Committees
Part IIReimagining Health Research Regulation
Section IIAPrivate and Public Dimensions of Health Research Regulation
28When Learning Is Continuous: Bridging the Research–Therapy Divide in the Regulatory Governance of Artificial Intelligence as Medical Devices
29The Oversight of Clinical Innovation in a Medical Marketplace
30The Challenge of ‘Evidence’: Research and Regulation of Traditional and Non-Conventional Medicines
31Experiences of Ethics, Governance and Scientific Practice in Neuroscience Research
32Humanitarian Research: Ethical Considerations in Conducting Research during Global Health Emergencies
33A Governance Framework for Advanced Therapies in Argentina: Regenerative Medicine, Advanced Therapies, Foresight, Regulation and Governance
Section IICTowards Responsive Regulation
35Towards a Global Germline Ethics? Human Heritable Genetic Modification and the Future of Health Research Regulation
36Cells, Animals and Human Subjects: Regulating Interspecies Biomedical Research
38A Perfect Storm: Non-evidence-Based Medicine in the Fertility Clinic
39Medical Devices Regulation: New Concepts and Perspectives Needed
Afterword: What Could a Learning Health Research Regulation System Look Like?