Which Of Following Protocols Is The One That Is Most Likely To Require IRB Review?
When conducting research involving human participants, it’s important to adhere to all applicable rules and regulations to ensure the safety of participants. One such regulation is the requirement for Institutional Review Board (IRB) approval of research protocols. IRB review is often necessary for protocols involving vulnerable populations or interventions that could present risks to participants.
What Protocols Require IRB Review?
The protocols most likely to require IRB review include those involving the use of data from medical records, surveys or interviews that will be used to draw conclusions about individuals, protocols that involve the use of any biological material from individuals or protocols that involve the introduction of any kind of drug, device or procedure that could potentially harm participants. In addition, any protocol involving deception or the risk of psychological harm to participants is likely to require IRB review.
The IRB Process
The IRB review process involves a review and approval of the research protocol prior to the start of the study. The IRB is responsible for ensuring that the proposed research meets all applicable ethical standards and guidelines. The IRB will review the research protocol to ensure that it is designed to protect the rights and welfare of the participants. They will also review the consent form to ensure that all information is provided in a manner that is easy to understand and that all risks associated with the research are clearly outlined.
Conclusion
The protocols most likely to require review by an IRB include protocols involving the use of data from medical records, surveys or interviews, the use of any biological material from individuals, the introduction of any kind of drug, device or procedure that could potentially harm participants and any protocol involving deception or the risk of psychological harm to participants. It is important to carefully review the protocol prior to conducting the study to ensure that it meets all applicable ethical standards and guidelines.