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Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Disclosure Personal Autonomy Confidentiality Patient Advocacy Patient Rights Informed Consent By Minors Patient Education as Topic Truth Disclosure Privacy Child Advocacy Government Regulation Duty to Warn Liability, Legal Treatment Refusal Malpractice Public Opinion Jurisprudence Therapeutic Misconception Internationality National Institutes of Health (U.S.)Genetic Privacy Defensive Medicine Human Rights Compensation and Redress Parents Judicial Role Freedom United States Office of Research Integrity Access to Information Federal Government War Crimes Cultural Diversity Family United States Dept. of Health and Human Services Physician Impairment United States Food and Drug Administration Developing Countries Social Justice Duty to Recontact Organizational Policy

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Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Third-Party Consent Ethics, Research Ethics Committees, Research Personal Autonomy Ethics, Medical Biological Specimen Banks Confidentiality Patient Advocacy Patient Rights Informed Consent By Minors Clinical Trials as Topic Ethics, Clinical Patient Selection Patient Participation Conflict of Interest Patient Education as Topic Physician-Patient Relations Ethical Review Privacy Child Advocacy Questionnaires Helsinki Declaration Ethics Committees Professional Staff Committees Government Regulation Randomized Controlled Trials as Topic Tissue Banks Duty to Warn Liability, Legal Prospective Studies Tissue and Organ Procurement Treatment Refusal Treatment Outcome Research Support as Topic Health Knowledge, Attitudes, Practice Risk Assessment Malpractice Guidelines as Topic Voluntary Programs Ethics Bioethics Jurisprudence Selection Bias Codes of Ethics Ethics, Professional Reproducibility of Results Clinical Trials, Phase I as Topic Pilot Projects National Institutes of Health (U.S.)Genetic Privacy Defensive Medicine Patient Satisfaction Data Collection Attitude to Health Clinical Trials Data Monitoring Committees Human Rights Sensitivity and Specificity Compensation and Redress Records as Topic Double-Blind Method Freedom Cross-Sectional Studies Risk Factors United States Office of Research Integrity Clinical Protocols Multicenter Studies as Topic Attitude of Health Personnel Clinical Trials, Phase IV as Topic Patient Identification Systems Medical Records Focus Groups Interviews as Topic Practice Guidelines as Topic Federal Government Feasibility Studies Genetic Testing Forms and Records Control Consumer Participation Mass Screening Educational Status Follow-Up Studies Retrospective Studies Observer Variation Institute of Medicine (U.S.)Hospitals, Teaching Legislation, Medical Emergencies Nursing Research Statistics, Nonparametric United States Dept. of Health and Human Services Single-Blind Method Physician Impairment Societies, Medical Clinical Trials, Phase III as Topic United States Food and Drug Administration Logistic Models Donor Selection Predictive Value of Tests Professional-Patient Relations Patient Acceptance of Health Care Cohort Studies Social Justice Guideline Adherence Physicians Duty to Recontact Organizational Policy

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Informed Consent Consent Forms Presumed Consent Parental Consent Mental Competency Research Subjects Human Experimentation Third-Party Consent Ethics, Research Disclosure Therapeutic Human Experimentation Nontherapeutic Human Experimentation Comprehension Ethics Committees, Research Personal Autonomy Ethics, Medical Beneficence Biomedical Research Minors Biological Specimen Banks Genetic Research Confidentiality Refusal to Participate Patient Advocacy Patient Rights Informed Consent By Minors Paternalism Research Personnel Clinical Trials as Topic Ethics, Clinical Decision Making Patient Selection Researcher-Subject Relations Research Design Legal Guardians Patient Participation Conflict of Interest Patient Education as Topic Bioethical Issues Truth Disclosure Physician-Patient Relations Ethical Review Privacy Child Advocacy Questionnaires Helsinki Declaration Ethics Committees Professional Staff Committees Government Regulation Randomized Controlled Trials as Topic United States Tissue Banks Communication Duty to Warn Liability, Legal Prospective Studies Tissue and Organ Procurement Morals Vulnerable Populations Treatment Refusal Moral Obligations Persons Treatment Outcome Research Support as Topic Health Knowledge, Attitudes, Practice Research Documentation Risk Assessment Malpractice Trust Public Opinion Guidelines as Topic Voluntary Programs Ethics Bioethics Jurisprudence Therapeutic Misconception Selection Bias Audiovisual Aids Control Groups AIDS Serodiagnosis Codes of Ethics Ethics, Professional Reproducibility of Results Internationality Clinical Trials, Phase I as Topic Pilot Projects National Institutes of Health (U.S.)Therapeutic Equipoise Genetic Privacy Information Dissemination Mentally Ill Persons Great Britain Defensive Medicine Patient Satisfaction Multimedia Patients Attitude Data Collection Attitude to Health

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