The Changing Clinical Trials Scene: The Role of the IRB
Mitchell, Shiela C.
IRB: A Review of Human Subjects Research. 1988 Jul/Aug; 10(4): 1-5.
Aids; Clinical Ethics; Clinical Ethics Committees; Clinical Trials; Control Groups; Critically Ill; Consent; Drugs; Ethical Review; Ethics; Ethics Committees; Federal Government; Food; Government; Heart Diseases; Human Experimentation; Incentives; IRB; Patient Care; Patients; Placebos; Random Selection; Regulation; Remuneration; Research; Research Design; Research Ethics; Research Ethics Committees; Research Subjects; Review; Selection of Subjects; Socioeconomic Factors; Terminally Ill; Therapeutic Research; Third Party Consent;
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