Informed consent聽is a crucial part of human subjects research. It is your responsibility as a researcher to ensure that all your study participants understand what they are agreeing to. These workshops will聽teach you how to obtain truly聽informed聽consent. Part 2: The... Read More
This training session covers a basic overview of the IRB, how to prepare a submission, helpful hints, and a demonstration of I-Manager. Repeats approximately monthly.
In some circumstances, alterations or waivers of consent can be appropriate and necessary to conduct research. Learn when and how to request alterations and waivers of consent.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.
Deadline for studies involving more than minimal risk to be reviewed at the next IRB meeting. Minimal risk studies are reviewed on an ongoing basis and may be submitted at any time.