What are the Key Considerations for IRBs in Toxicology Studies?
Given the potential risks associated with toxicological research, IRBs focus on several key areas:
Risk-Benefit Analysis: Evaluating whether the potential benefits of the research outweigh the risks to participants. Informed Consent: Ensuring that participants are fully informed about the nature of the study, including potential risks and benefits. Participant Selection: Ensuring that the selection of participants is equitable and just, and that vulnerable populations are protected. Monitoring and Reporting: Ensuring that there are mechanisms in place for ongoing monitoring of the study and that any adverse events are promptly reported and addressed.
