Research and IRB

This paper concentrates on the primary theme of Research and IRB in which you have to explain and evaluate its intricate aspects in detail. In addition to this, this paper has been reviewed and purchased by most of the students hence; it has been rated 4.8 points on the scale of 5 points. Besides, the price of this paper starts from £ 79. For more details and full access to the paper, please refer to the site.

Research and IRB

Can someone please help with this response. I need to answer ONE of the following questions and I am at a loss. I cannot find many informative references to arrive at a conclusion. It does not need to be a long answer, just a good starting point.


You are conducting a randomized clinical trial to evaluate a new chemotherapy regimen for treatment of inoperable non-small-cell lung cancer. Patients with inoperable lung cancer will be randomized to the new regimen or no active care. It is hoped that the new regimen will improve disease-free survival and overall survival.

What evidence will the Committee on Human Subjects (IRB) require before approving your protocol?


What training would you provide to the people obtaining informed consent?


What material should be included in the informed consent form?

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