Trudo Lemmens – författare

Since legalizing euthanasia and assisted suicide as medical assistance in dying (MAiD) in 2016, Canada has witnessed an internationally unprecedented expansion of the practice, making it the country with the highest number of MAiD deaths.Initially introduced to relieve suffering in a broad end-of-life context, the law expanded quickly to make MAiD available to disabled Canadians not approaching their natural deaths. MAID will also become legal for sole reasons of mental illness sometime after 2027, and there are plans to expand it further to include minors and advance requests. From a cross-disciplinary perspective, including contributions from authors with lived experience, Indigenous perspectives, and expertise in medicine, mental health, disability, law, and ethics, Unravelling MAiD in Canada challenges readers with the ethical, medical, legal, societal, and disability justice rights concerns that have arisen in regard to this hotly debated irreversible practice.Canada now provides more state-facilitated euthanasia and assisted suicide than any other country. This volume puts forth critical reflections and valuable insights as more jurisdictions consider their own assisted dying laws and policies.

When a young man named Jesse Gelsinger died in 1999 as a result of his participation in a gene transfer research study, regulatory agencies in the United States began to take a closer look at what was happening in medical research. The resulting temporary shutdown of some of the most prestigious academic research centres confirmed what various recent reports in the United States as well as Canada had claimed; that the current system of regulatory oversight was in need of improvement.Law and Ethics in Biomedical Research uses the Gelinger case as a touchstone, illustrating how three major aspects of that case - the flaws in the regulatory system, conflicts of interest, and legal liability - embody the major challenges in the current medical research environment. Editors Trudo Lemmens and Duff R. Waring, along with a host of top scholars in the field, demonstrate why existing models of research review and human subject protection are in need of improvement, and how more stringent regulatory and legal means can be used to strengthen the protection of research subjects and the integrity of research.The contributors also address conflicts of interest, paying particular attention to the growing commercialization of medical research, as well as the legal liability of scientific investigators, research institutions, and governmental agencies. Legal liability is a growing concern in medical research and this fascinating study is, in the international context, one of the first to explore the liability of various parties involved in the research enterprise.

In 2004, the Assisted Human Reproduction Act was passed by the Parliament of Canada. Fully in force by 2007, the act was intended to safeguard and promote the health, safety, dignity, and rights of Canadians. However, a 2010 Supreme Court of Canada decision ruled that key parts of the act were invalid.Regulating Creation is a collection of essays built around the 2010 ruling. Featuring contributions by Canadian and international scholars, it offers a variety of perspectives on the role of law in dealing with the legal, ethical, and policy issues surrounding changing reproductive technologies.  In addition to the in-depth analysis of the Canadian case the volume reflects on how other countries, particularly the U.S., U.K. and New Zealand regulate these same issues.  Combining a detailed discussion of legal approaches with an in-depth exploration of societal implications, Regulating Creation deftly navigates the obstacles of legal policy amidst the rapid current of reproductive technological innovation.