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The book is divided thematically into three sections, where the first deals with foundational and general issues of health law, the second with patients’ rights, and the third with issues related to advancements in biomedical science.
The first part includes two chapters on the relationship between health law and human rights, together with discussions on specific Nordic approaches to the organisation and regulation of health services, to constitutional protection of the right to health and to the legal discipline of health law, as such. One chapter provides an overview of the mission and tasks of the Nordic Committee on Bioethics.
The section on patient’s rights deals with the development – or absence – of special legislation on the status of patients, but also with issues of coercive care and of cultural accommodation in health services, as well as the implications that assessments and decisions made in health care services may have for the patient’s right to other entitlements, e.g. sickness benefits.
In the third section, on biomedical science, one author explores the concept of human dignity while another discusses the challenges facing European integration of biomedical research regulation. Specific topics, such as different approaches to biobank regulation and genetic privacy in family relations, are also addressed, and, in the final chapter, the legal status of deceased foetuses.
While the anthology thus in part provides specifically Nordic perspectives on health law, the issues discussed are at the same time general. The book is therefore well suited not only to readers who want a better understanding of the Nordic situation, but also to anyone with an interest in the challenging health law issues facing society in our time.