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Bioethics --- Bioethics. --- Bioethical Issues. --- Patient Rights. --- Case Reports. --- Bioethical issues. --- Bioethical Issues --- Patient Rights --- Patient's Rights --- Patients' Rights --- Right to Treatment --- Patient Right --- Patient's Right --- Patients Rights --- Patients' Right --- Right to Treatments --- Right, Patient --- Right, Patient's --- Right, Patients' --- Rights, Patient --- Rights, Patient's --- Rights, Patients' --- Treatment, Right to --- Treatments, Right to --- Bioethical Issue --- Issue, Bioethical --- Issues, Bioethical --- Biomedical Ethics --- Health Care Ethics --- Ethics, Biomedical --- Ethics, Health Care --- Biology --- Biomedical ethics --- Life sciences --- Life sciences ethics --- Moral and ethical aspects --- Patient Advocacy --- Truth Disclosure --- Euthanasia --- Human Experimentation --- Animal Experimentation --- Ethics, Medical --- Ethicists --- Science

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Mental health laws --- Insanity (Law) --- Forensic Psychiatry --- Jurisprudence --- Mental Health --- Patient Rights --- Mental health laws. --- Insane --- Mentally ill --- Law and mental illness --- Mental disability law --- Mental health --- Mental illness and law --- Mental illness --- People with mental disabilities --- Criminal insanity --- Insanity --- Lunacy (Law) --- Capacity and disability --- Insanity defense --- Patient's Rights --- Patients' Rights --- Right to Treatment --- Patient Right --- Patient's Right --- Patients Rights --- Patients' Right --- Right to Treatments --- Right, Patient --- Right, Patient's --- Right, Patients' --- Rights, Patient --- Rights, Patient's --- Rights, Patients' --- Treatment, Right to --- Treatments, Right to --- Patient Advocacy --- Truth Disclosure --- Bioethical Issues --- Mental Hygiene --- Health, Mental --- Hygiene, Mental --- Orthopsychiatry --- Constitutional Law --- Court Decision --- Law --- Legal Aspects --- Legal Obligations --- Legal Status --- State Interest --- Litigation --- Medical Jurisprudence --- Aspect, Legal --- Aspects, Legal --- Constitutional Laws --- Court Decisions --- Decision, Court --- Decisions, Court --- Interest, State --- Interests, State --- Jurisprudence, Medical --- Law, Constitutional --- Laws --- Laws, Constitutional --- Legal Aspect --- Legal Obligation --- Litigations --- Obligation, Legal --- Obligations, Legal --- State Interests --- Status, Legal --- Defamation --- Lawyers --- Jurisprudence, Psychiatric --- Psychiatric Jurisprudence --- Psychiatry, Forensic --- Insanity (Jurisprudence) --- Law and legislation --- Legal status, laws, etc. --- United Kingdom --- Great Britain. --- Anglia --- Angliyah --- Briṭanyah --- England and Wales --- Förenade kungariket --- Grã-Bretanha --- Grande-Bretagne --- Grossbritannien --- Igirisu --- Iso-Britannia --- Marea Britanie --- Nagy-Britannia --- Prydain Fawr --- Royaume-Uni --- Saharātchaʻānāčhak --- Storbritannien --- United Kingdom of Great Britain and Ireland --- United Kingdom of Great Britain and Northern Ireland --- Velikobritanii͡ --- Wielka Brytania --- Yhdistynyt kuningaskunta --- Northern Ireland --- Scotland --- Wales --- Great Britain --- Isle of Man --- Law - Great Britain --- Health Sciences --- Psychiatry & Psychology --- General and Others

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As the prospect of a legal right to advocacy inches closer, so the need to scrutinise its key values and practices becomes urgent. Although widely acclaimed as a 'good thing', there is little agreement as to how advocacy should be implemented, funded or evaluated. This book offers the first comprehensive analysis of the benefits of advocacy.

Health & Biological Sciences. --- Medicine. --- Medical Professional Practice. --- Patients --- Patient advocacy. --- MEDICAL --- Anthropology, Education, Sociology and Social Phenomena. --- Social Sciences. --- Health Care. --- Health Care Economics and Organizations. --- Sociology. --- Policy. --- Social Control, Formal. --- Social Control Policies. --- Public Policy. --- Patient Advocacy. --- Human Rights. --- Patient advocacy --- Civil rights. --- Health Policy. --- Health Risk Assessment. --- Civil rights --- Great Britain. --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Patients' rights --- Health Workforce --- Persons --- Sick --- Basic rights --- Civil rights (International law) --- Human rights --- Rights, Human --- Rights of man --- Human security --- Transitional justice --- Truth commissions --- Social theory --- Social sciences --- Delivery of health care --- Delivery of medical care --- Health care --- Health care delivery --- Health services --- Healthcare --- Medical and health care industry --- Medical services --- Personal health services --- Public health --- Behavioral sciences --- Human sciences --- Sciences, Social --- Social science --- Social studies --- Civilization --- Quality control --- Law and legislation

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In het kader van de Leerstoel Rector Dhanis (UFSIA, Antwerpen) werd door een studiegroep bestaande uit artsen en verpleegkundigen, ethici en juristen, een interdisciplinaire studie ondernomen over 'klinische ethiek' en 'hoe recht en politiek omgaan met problemen die thuishoren in de klinische praktijk'. In deze bundel wordt het ethische denken in een aantal casussen betreffende neonatalen en dementerenden kritisch besproken. De adviezen van het Raadgevend Comité voor Bio-Ethiek over sterilisatie van mentaal gehandicapten en over klonering worden onderzocht op hun relevantie voor de klinische praktijk.

ouderschap --- euthanasie --- Natural law --- gezondheidsrecht --- Professional ethics. Deontology --- medische ethiek --- Medical law --- baby's --- Ethique médicale --- Medische ethiek --- WB 60 Bioethics. Clinical ethics. Clinical ethics committees --- Medical ethics. --- Bioethics. --- Patients --- Legal status, laws, etc. --- 17.023.33 <493> --- #GGSB: Bio-ethiek --- #GGSB: Moraal - Algemeen --- 061 Ethische problemen --- ethiek --- medisch recht --- 603.1 --- bio-ethiek --- casestudies --- filosofie --- klonen --- mentaal gehandicapten --- neonatologie --- prenatale diagnose --- recht --- sterilisatie --- voeding --- wilsonbekwaamheid --- autonomie --- biotechnologie --- geboorteregeling (anticonceptie) --- lichaamsbeeld --- pasgeborenen --- Biologische doeleinden. Bio-ethiek; bioethiek. Übermensch. Medische deontologie--België --- (zie ook: terminale zorgen) --- (zie ook: zwakzinnigheid) --- (zie ook: genetisch advies) --- 17.023.33 <493> Biologische doeleinden. Bio-ethiek; bioethiek. Übermensch. Medische deontologie--België --- Bioethics --- Medical ethics --- C6 --- Patients' rights --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Professional ethics --- Nursing ethics --- Social medicine --- Biology --- Life sciences --- Life sciences ethics --- Science --- Legal status, laws, etc --- Opvoeding, onderwijs, wetenschap --- Moral and ethical aspects --- Biologische doeleinden. Bio-ethiek; bioethiek. Übermensch. Medische deontologie--België --- Bio-ethiek --- Moraal - Algemeen --- Patients - Legal status, laws, etc.

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Outlines an approach to ensure the protection of participants through the establishment of effective Human Research Participant Protection Programs (HRPPP). Topics covered in this book include improved research review processes, recognition and integration of research participants contributions to the system, and vigilant maintenance of HRPPP performance. When 18-year-old Jesse Gelsinger died in a gene transfer study at the University of Pennsylvania, the national spotlight focused on the procedures used to ensure research participants safety and their capacity to safeguard the well-being of those who volunteer for research studies. "Responsible Research" outlines a three-pronged approach to ensure the protection of every participant through the establishment of effective Human Research Participant Protection Programs (HRPPPs). The approach includes: improved research review processes; recognition and integration of research participants contributions to the system, and vigilant maintenance of HRPPP performance. Issues addressed in the book include the need for in-depth, complimentary reviews of science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal and institutional oversight; and the role of accreditation. Recommendations for areas of key interest include suggestions for legislative approaches, compensation for research-related injury, and the refocusing of the mission of institutional review boards. "Responsible Research" will be important to anyone interested in the issues that are relevant to the practice of using human subjects as research participants, but especially so to policy makers, research administrators, investigators, and research sponsors but also including volunteers who may agree to serve as research participants.

MEDICAL --- Research --- Ethics --- Human Rights --- Epidemiologic Study Characteristics as Topic --- Jurisprudence --- Professional-Patient Relations --- Investigative Techniques --- Social Control Policies --- Biomedical Research --- Accident Prevention --- Persons --- Social Control, Formal --- Professional Staff Committees --- Ethics Committees --- Therapeutics --- Health Care Quality, Access, and Evaluation --- Policy --- Health Care Economics and Organizations --- Named Groups --- Humanities --- Interpersonal Relations --- Accidents --- Sociology --- Quality Assurance, Health Care --- Health Care Evaluation Mechanisms --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Science --- Professional Practice --- Quality of Health Care --- Health Care --- Social Sciences --- Public Health --- Psychology, Social --- Natural Science Disciplines --- Disciplines and Occupations --- Anthropology, Education, Sociology and Social Phenomena --- Organization and Administration --- Environment and Public Health --- Behavior and Behavior Mechanisms --- Psychiatry and Psychology --- Health Services Administration --- Human Experimentation --- Safety --- Government Regulation --- Public Policy --- Conflict of Interest --- Ethics Committees, Research --- Informed Consent --- Clinical Protocols --- Researcher-Subject Relations --- Ethical Review --- Patient Rights --- Clinical Trials Data Monitoring Committees --- Research Subjects --- experiment, experimenteel onderzoek (mensen) --- ethiek (ethische aspecten) --- geïnformeerde vrijwillige toestemming (instemming) --- proefpersonen --- Verenigde Staten --- belangenconflict --- expérimentation sur la personne humaine (chez l'humain) --- ethique (aspects ethiques) --- consentement libre et éclairé --- sujets (participants) d'expérimentation --- Etats Unis --- conflit d'intérêt --- Human experimentation in medicine --- Medical ethics. --- Medical protocols. --- Patients --- Moral and ethical aspects. --- Legal status, laws, etc. --- Patients' rights --- Clinical algorithms --- Clinical protocols --- Patient care plans --- Plans for patient care --- Protocols in medicine --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Moral and ethical aspects --- Clinical medicine --- Medical records --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Medical ethics --- Medical protocols --- Legal status, laws, etc