Any research that does not fit into the exempt or expedited review categories must go to full-board review. 这包括IRB认为涉及的任何研究 大于最小风险。

To obtain full-board review, the research requires approval from a majority of IRB members present at a full-board meeting. The UVU IRB meets once per month to review full-board applications. 每月的会议时间表可以在我们的主页上找到。 Investigators are invited, an encouraged to attend, the meeting review of their application to answer questions and address committee concerns.

IRB duties are described in the Federal Regulation for Protection of Human Subjects (45 CFR 46).

全面研究的例子

• Clinical procedures with drugs, devices, or biologics, or innovative research into new medical, behavioral, or surgical procedures (Clinical Trials)
• Research taking place internationally (particularly countries with little or no provisions for protection of human subjects) where subjects may be at physical, psychological or legal risk (NOTE, international research must first be approved by the ethics board of the forgien country before they can be reviewed by UVU IRB)
• 大多数项目都涉及欺骗
• Majority of projects involving vulnerable populations (Prisoner, children, and neonates, per federal regulation)