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Animals, Laboratory Candida

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International Normalized Ratio Human Experimentation Treatment Outcome Reference Standards Clinical Trials as Topic Questionnaires Risk Factors Reproducibility of Results Retrospective Studies Immunization Schedule Animal Experimentation Research Design Prognosis Multicenter Studies as Topic Data Collection Prospective Studies Risk Assessment Nontherapeutic Human Experimentation Registries Follow-Up Studies Prevalence Survival Analysis Population Surveillance Drug Approval Randomized Controlled Trials as Topic Neoplasm Staging Severity of Illness Index Vaccination Incidence Cohort Studies Microbial Sensitivity Tests Sensitivity and Specificity Cross-Sectional Studies Clinical Protocols Survival Rate Prothrombin Time Therapeutic Human Experimentation Disease-Free Survival Predictive Value of Tests Disability Evaluation Patient Selection Combined Modality Therapy Evaluation Studies as Topic Double-Blind Method Antineoplastic Combined Chemotherapy Protocols Records as Topic Biological Assay Multivariate Analysis Program Evaluation Drug Administration Schedule Pilot Projects Health Surveys Clinical Laboratory Techniques Risk

Psychiatry and Psychology11

Consensus Peer Review, Research Dissent and Disputes Cooperative Behavior Peer Review Confidentiality Decision Making Leadership Interdisciplinary Communication Disclosure Erectile Dysfunction

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Time Factors Mutation Phenotype Sensitivity and Specificity Pregnancy Prothrombin Time Genotype Risk

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International Classification of Diseases Terminology as Topic Questionnaires Data Collection International Classification of Functioning, Disability and Health Publishing Databases, Factual Editorial Policies Registries Prevalence Consensus Development Conferences as Topic Authorship Periodicals as Topic Delphi Technique Incidence Information Dissemination Survival Rate Peer Review, Research Molecular Sequence Data Internet Records as Topic Research Report Documentation Bibliometrics Translations Interdisciplinary Communication Disclosure Classification

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Ethics Committees Committee Membership Advisory Committees Ethics Committees, Research International Agencies Professional Staff Committees Ethics Committees, Clinical Ethical Review Pharmacy and Therapeutics Committee Clinical Trials Data Monitoring Committees Societies, Medical World Health Organization Rescue Work World Health Guidelines as Topic Congresses as Topic Ethics, Research Treatment Outcome Ethics Consultation Practice Guidelines as Topic Foreign Medical Graduates Ethics, Medical Health Planning Guidelines Clinical Trials as Topic Societies, Scientific Questionnaires Risk Factors Reproducibility of Results Retrospective Studies Social Control, Formal Health Policy Government Regulation United Nations Multicenter Studies as Topic Human Rights Data Collection Prospective Studies Risk Assessment Laboratories Public Policy American Medical Association Societies Informed Consent Public Health United States Food and Drug Administration Registries Follow-Up Studies Prevalence Survival Analysis Ethicists Consensus Development Conferences as Topic Conflict of Interest Population Surveillance Age Factors Red Cross Randomized Controlled Trials as Topic Academies and Institutes Severity of Illness Index Vaccination Communicable Disease Control Research Support as Topic Incidence Cohort Studies Ethics, Institutional Sensitivity and Specificity Cross-Sectional Studies Clinical Protocols Accreditation Survival Rate Program Development Peer Review, Research Quality Assurance, Health Care Policy Making Organizational Policy Government Agencies Bioethics Guideline Adherence Outcome Assessment (Health Care)Organizations Delivery of Health Care Centers for Disease Control and Prevention (U.S.)Disease-Free Survival Peer Review Patient Rights American Heart Association Consumer Advocacy Confidentiality Helsinki Declaration Predictive Value of Tests Health Planning Councils Licensure Disease Outbreaks Patient Selection Institute of Medicine (U.S.)Consent Forms Evaluation Studies as Topic Decision Making, Organizational Federal Government Cost-Benefit Analysis Expert Testimony Double-Blind Method Sex Factors Immunization Programs Policy Certification Financing, Organized Organizational Objectives Safety National Institutes of Health (U.S.)Emigration and Immigration Records as Topic Multivariate Analysis International Council of Nurses Nursing Government Program Evaluation National Health Programs Clinical Competence Relief Work Health Promotion Pilot Projects Health Services Research Health Surveys Benchmarking Hospitals Physician's Practice Patterns Health Personnel Costs and Cost Analysis Risk

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International Cooperation Ethics Committees Committee Membership Advisory Committees Ethics Committees, Research International Agencies Professional Staff Committees Ethics Committees, Clinical Ethical Review Internationality Animal Care Committees Pharmacy and Therapeutics Committee International Normalized Ratio International Classification of Diseases Clinical Trials Data Monitoring Committees Societies, Medical Terminology as Topic World Health Organization United States Rescue Work Europe International Educational Exchange World Health Guidelines as Topic Congresses as Topic Ethics, Research Human Experimentation Treatment Outcome Biomedical Research Ethics Consultation Consensus Canada European Union Practice Guidelines as Topic History, 20th Century Foreign Medical Graduates Great Britain Reference Standards Ethics, Medical Research Health Planning Guidelines Clinical Trials as Topic Societies, Scientific Developing Countries Quality Control Questionnaires Time Factors Risk Factors Reproducibility of Results Retrospective Studies Social Control, Formal Health Policy Immunization Schedule Animal Experimentation Research Design Government Regulation United Nations Travel Prognosis Multicenter Studies as Topic Human Rights Data Collection Prospective Studies International Classification of Functioning, Disability and Health Risk Assessment Laboratories Australia Public Policy American Medical Association Societies Informed Consent Public Health Mutation Publishing Nontherapeutic Human Experimentation Evidence-Based Medicine Databases, Factual Bioethical Issues Editorial Policies Cross-Cultural Comparison Japan United States Food and Drug Administration Politics Developed Countries Registries Follow-Up Studies Prevalence Research Subjects Infant, Newborn Survival Analysis Ethicists Consensus Development Conferences as Topic Conflict of Interest Population Surveillance Phenotype Research Personnel Age Factors Authorship Drug Industry History, 21st Century

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