Circumstances template informed consent. Medical search. Frequent questions

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Organisms1

Escherichia coli

Diseases4

Death Neoplasms Emergencies HIV Infections

Chemicals and Drugs10

DNA-Directed RNA Polymerases DNA-Directed DNA Polymerase DNA RNA, Viral RNA RNA-Directed DNA Polymerase RNA Replicase DNA, Viral DNA, Single-Stranded DNA Polymerase I

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Patient Selection Clinical Trials as Topic Questionnaires Research Design Randomized Controlled Trials as Topic Prospective Studies Risk Assessment AIDS Serodiagnosis Sensitivity and Specificity Reproducibility of Results Control Groups Pilot Projects Surgical Procedures, Operative Treatment Outcome Cross-Sectional Studies Risk Factors Records as Topic Interviews as Topic Data Collection Clinical Trials, Phase I as Topic Surgical Procedures, Elective Medical Records Clinical Trials, Phase IV as Topic Focus Groups Magnetic Resonance Imaging Embryo Disposition Genetic Testing Retrospective Studies Feasibility Studies Models, Molecular Clinical Protocols Polymerase Chain Reaction Mass Screening Image Interpretation, Computer-Assisted Logistic Models Resuscitation Donor Selection Cohort Studies Follow-Up Studies

Psychiatry and Psychology31

Mental Competency Disclosure Comprehension Personal Autonomy Confidentiality Refusal to Participate Paternalism Decision Making Physician-Patient Relations Truth Disclosure Researcher-Subject Relations Communication Duty to Warn Morals Treatment Refusal Health Knowledge, Attitudes, Practice Trust Ethics Attitude to Health Attitude Parents Mental Recall Attitude of Health Personnel Focus Groups Professional-Family Relations Family Behavioral Research Altruism Social Values Professional-Patient Relations Duty to Recontact

Phenomena and Processes12

Templates, Genetic Base Sequence Transcription, Genetic DNA Replication Sensitivity and Specificity Time Factors Pregnancy Kinetics Nucleic Acid Conformation Algorithms Mutation DNA, Single-Stranded

Disciplines and Occupations14

Human Experimentation Therapeutic Human Experimentation Nontherapeutic Human Experimentation Biomedical Research Genetic Research Research Design Empirical Research Emergency Medicine Research Qualitative Research General Surgery Anesthesiology Behavioral Research Pediatrics

Anthropology, Education, Sociology and Social Phenomena44

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 Truth Disclosure Patient Education as Topic Privacy Child Advocacy Duty to Warn Government Regulation Liability, Legal Treatment Refusal Malpractice Public Opinion Jurisprudence Therapeutic Misconception Internationality Human Rights Genetic Privacy Parents Defensive Medicine Judicial Role Freedom United States Office of Research Integrity Compensation and Redress Family War Crimes Socioeconomic Factors Access to Information Social Justice Cultural Diversity Developing Countries Federal Government Physician Impairment Duty to Recontact Advance Directives

Technology, Industry, Agriculture2

Audiovisual Aids Multimedia

Humanities23

Ethics, Research Personal Autonomy Ethics, Medical Beneficence Ethics Committees, Research Ethics, Clinical Bioethical Issues Helsinki Declaration Conflict of Interest Ethical Review Ethics Committees Moral Obligations Morals Bioethics Ethics Therapeutic Misconception Codes of Ethics Ethics, Professional Therapeutic Equipoise Social Responsibility Principle-Based Ethics Social Justice Religion and Medicine

Information Science22

Disclosure Questionnaires Communication Base Sequence Molecular Sequence Data Documentation Audiovisual Aids Multimedia Information Dissemination Records as Topic Interviews as Topic Data Collection Medical Records Focus Groups Access to Information Algorithms Image Interpretation, Computer-Assisted Pamphlets Communication Barriers Journalism, Medical Internet Editorial Policies

Named Groups13

Research Subjects Minors Legal Guardians Vulnerable Populations Research Personnel Persons Mentally Ill Persons Parents Patients Pregnant Women Tissue Donors Infant, Newborn Physicians

Health Care100

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

Geographicals5

United States Great Britain India Canada Germany, West

Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Technology, Industry, Agriculture Humanities Information Science Named Groups Health Care Geographicals

Informed Consent Consent Forms Templates, Genetic Presumed Consent Parental Consent Mental Competency Research Subjects Human Experimentation Third-Party Consent Disclosure Ethics, Research Therapeutic Human Experimentation Nontherapeutic Human Experimentation Comprehension Personal Autonomy Ethics, Medical Beneficence Minors Ethics Committees, Research Biological Specimen Banks Biomedical Research Confidentiality Genetic Research Refusal to Participate Patient Advocacy Paternalism Patient Rights Informed Consent By Minors Decision Making Ethics, Clinical Patient Selection Clinical Trials as Topic Legal Guardians Patient Participation Physician-Patient Relations Truth Disclosure Patient Education as Topic Researcher-Subject Relations Bioethical Issues Privacy Child Advocacy Questionnaires Helsinki Declaration Research Design Conflict of Interest Communication Ethical Review Duty to Warn Government Regulation Ethics Committees Moral Obligations Morals Tissue and Organ Procurement Liability, Legal Professional Staff Committees Treatment Refusal United States Vulnerable Populations Tissue Banks Research Personnel Base Sequence Persons Randomized Controlled Trials as Topic Prospective Studies Molecular Sequence Data Documentation Great Britain Malpractice Public Opinion Bioethics Jurisprudence Health Knowledge, Attitudes, Practice Risk Assessment Trust Transcription, Genetic Ethics Voluntary Programs Mentally Ill Persons Guidelines as Topic DNA-Directed RNA Polymerases Therapeutic Misconception DNA Replication Audiovisual Aids AIDS Serodiagnosis Codes of Ethics Internationality DNA-Directed DNA Polymerase Ethics, Professional Sensitivity and Specificity Time Factors Attitude to Health Therapeutic Equipoise DNA Human Rights Genetic Privacy Attitude Reproducibility of Results Social Responsibility Parents Control Groups

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