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Clinical Trials Ethics
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Flashcards
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Placebo Use
The ethical considerations in using a placebo in clinical trials, which may involve withholding treatment from a control group.
Post-Trial Access
The ethical obligation to provide continued access to beneficial treatments or interventions after the conclusion of a clinical trial.
Informed Consent
A process ensuring that a patient or participant is fully informed about the trial and understands the risks and benefits.
Risk-Benefit Analysis
Evaluation of the potential risks and anticipated benefits to determine if the research is ethically justifiable.
Vulnerable Populations
Special ethical considerations must be made for groups that may have limited capacity to consent or may be at higher risk of coercion or undue influence.
Confidentiality
Respecting the privacy of trial participants and maintaining the confidentiality of trial data.
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