Bioethics Information Nurses 
Advarra
MARCH 6, 2025
This is why IRBs are tasked with conducting an ethical review of clinical trial proposals to ensure participants are informed of risks before and during their participation in any trial. That is not to say that they do not face potential risks.
Codon
JANUARY 21, 2024
It introduced concepts like informed consent and risk/benefit analysis for clinical studies. I think there was still worthwhile information that came out of COVID challenge models, and there's plenty of future value, especially if we work on a broad-spectrum coronavirus family vaccine of some sort. That's what Josh was getting at.
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