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INTEGREVIEW IRB July 28, 2019 APPROVED

FUNDUS CAMERA STUDY Why we are doing this study: This study will be evaluating the accuracy and quality of retinal images using an investigational imaging device in participants with a history of diabetes. Who can be in the study? You may be eligible to participate if you are 22 years of age or over and have: • Diabetes • Without retinopathy • With diabetic retinopathy Further screening questions will be asked prior to scheduling an appointment. What the study involves: Participants will be screened with assessments typical of an eye examination (including dilation) to verify that the eye(s) meet the requirements to be grouped in one of the categories being studied. Eligible participants will have one or both eyes scanned with the investigational device as well as by 1 other FDA approved device.

The entire visit is expected to take up to 2 hours. Will you directly benefit from the study?

There is not expected to be any direct benefit. Other things you should know about the study: Participants will be compensated up to $100. Principal Investigator: Mitchell Dul, OD For more information, contact the Clinical Vision Research Center