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Frequently Asked Questions
Deciding whether or not to participate in a clinical trial/study is a difficult decision to make. To assist you, we have compiled a list of frequently asked questions and answers that may provide you with the information you need to make this important decision. The information below has been borrowed from the National Institutes of Health's cancer.gov website.
Who makes sure my rights are protected?
Groups of experts at the national and local levels approve research studies before they begin. One of the most important groups is called an institutional review board (IRB).
The IRB’s job is to review research studies and make sure that they are run safely and fairly. All clinical trials are reviewed and approved by an IRB, which includes doctors, nurses, and people from the community.
Back to Frequently Asked Questions page