Abstract
Australia has a federal government system where the central Commonwealth government in Canberra competes in the medical and health care fields with the six state governments -New South Wales, Victoria, Queensland, Western Australia, South Australia, Tasmania -and two territory governments -the Northern Territory and the Australian Capital Territory. As a result there are state laws and legal structures and organizations dealing with biœthical issues which are sometimes a variance with each other and also at variance with Commonwealth laws and structures.
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Bibliography
The Age, 1993, Melbourne, November 18.
Ashby, Michael, and Wakefield, Melanie: 1993.: “Attitudes to some aspects of death and dying, living wills and substituted health care decision making in South Australia”. Public opinion survey for a parliamentary select committee, Parliament of South Australia, Adelaide.
Brahams, Diana: 1991, “Australian mother sued by child injured in utero”, The Lancet, 338, pp. 687–8.
Chalmers, D., and Schwartz, R.: 1993, ”Rogers v.Whitaker and Informed Consent in Australia: A Fair Dinkum Duty of Disclosure”, Medical Law Review, 1, pp. 139–159,
Charlesworth, Max.; 1993, Bioethics in a Liberal Society, Cambridge University Press, Melbourne.
Choice or Chance? The Ethics of Resource Allocation for Minority Groups: 1993, Australian Health Ethics Committee, NHMRC, Canberra.
Cooper, Josephine: 1991, “Facing Up to the Duty of Surveillance: An Ongoing Relationship Between Institutional Ethics Committees and Researchers”, Bioethics News, Monash Centre for Human Bioethics. 10, July, pp. 3–10.
Distributing Health Care Resources: Ethical Assumptions: 1992, Australian Health Ethics Committee. NHMRC, GPO Box 9848, Canberra ACT 2601.
Ethics and Resource Allocation in Australian Health Care: 1992,Australian Health Ethics Committee, NHMRC, Canberra.
Ethical Considerations Relating to Health Care Resource Allocation Decisions: 1993, Australian Health Ethics Committee, NHMRC, Canberra.
Guidelines on Ethical Matters in Aboriginal and Torres Strait Islander Health Research: 1991, NHMRC, Canberra.
Health Services and Ethnic Communities: An Agenda for Change: 1991, Report of the Victorian Ministerial Taskforce on Ethnic Health.
Kovacs, G. T., Mushin, D., Kane, H., Baker, H. W. G.: 1993 “A controlled study of the psychosocial development of children conceived by insemination with donor semen”, Human Reproduction, 8.
Kuhse, H.: 1993, “Medically assisted suicide Bill”, Bioethics News, Monash Centre for Human Bioethics, October 12, p. 7.
Lane, Margaret J.: 1991: “Privacy protection and medical research: ethical and legal issues in public health”, Bioethics News, Monash University, October 11, pp. 3–10.
Legal liability, insurance and indemnity arrangements for Institutional Ethics Committees: 1993, Australian Health Ethics Committee, NHMRC.
Loblay R.: 1993, Use of Routine Blood and Tissue Samples for Research, Discussion paper for Australian Health Ethics Committee, Canberra, p. 1.
McNeill, Paul: 1993, The Ethics and Politics of Human Experimentation, Cambridge University Press, Melbourne.
Mendelson, D.: 1992, ”The Medical Treatment (Enduring Power of Attorney) Act and assisted suicide: the legal position in Victoria”, Bioethics News, October 12, pp. 34–42.
Monash Centre for Human Bioethics: 1989, The Fetus as Tissue Donor: Use or Abuse? Monash University, Melbourne.
Morgan Computer Reports: 1993, Sydney, No. 1222.
National Health and Medical Research Council: 1993, General Guidelines for Medical Practitioners on Providing Information to Patients, GPO Box 9848, Canberra, ACT.
The Place of Ethics in Health Care Resource Allocation: Where to Now?: 1992, Australian Health Ethics Committee, NHMRC, Canberra.
Reid, Janice and Trompf, Peggy: 1990, The Health of Immigrant Australia: A Social Perspective, Harcourt Brace, Jovanovich.
Rogers v. Whitaker (1992) 67 A.L.J.R. 47 (High Court of Australia).
Skene, L.: 1991, The Baby M Inquest: Treating Children with Severe Spina Bifida, Law Reform Commission of Victoria, Melbourne, Victoria.
Smallwood, R. A.: 1991, “Privacy laws and their effect on medical research”, The Medical Journal of Australia, 154, February 4, pp. 158–9.
South Australian Council on Reproductive Technology: 1993, Families by Donation: Donated eggs or sperm, does it make a difference to the family? Adelaide.
Standing Review and Advisory Committee on Infertility: 1991, Report to the Minister for Health on Matters Related to the “Review of ’post-syngamy’Embryo Experimentation”: Part III: Recommendations for amendment of the Infertility (Medical Procedures) Act 1984, Health Department of Victoria, Melbourne.
Stevens, Christine A., and Hassan, R.: 1993, Management of Death, Dying and Euthanasia; Attitudes and Practices of Medical Practitioners and Nurses in South Australia, School of Social Sciences, Flinders University, Adelaide.
Voluntary and Natural Death Bill, 1993. Copies of the Bill may be obtained from The Hon. Michael Moore MLA, Legislative Assembly for the Australian Capital Territory, I Constitution Avenue, Canberra, A.C.T. 2601.
Western Australian Reproductive Technology Council, Annual Report 1992–3, PO Box 81772, Stirling Street, Perth, WA., 6849.
Western Australian Reproductive Technology Council: 1993, Draft Guidelines.
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Charlesworth, M. (1995). Bioethics in Australia: 1991–1993. In: Lustig, B.A. (eds) Bioethics Yearbook. Bioethics Yearbook, vol 4. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0197-4_16
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DOI: https://doi.org/10.1007/978-94-011-0197-4_16
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