For continuing review of research that involves an intervention/interaction with human subjects. This form is to report progress of the study to-date. The PHRC must re-assess the risk-benefit ratio at intervals appropriate to the degree of risk associated with the study procedures, but not less then once per year.

Minor Violation Report
2/04

Protocol Summary
6/05

Summary document describing the protocol and the investigator's plan for recruitment and enrollment of subjects. Includes important regulatory information needed for IRB review.

For continuing review of research that is limited to the use of excess human material/specimens and related health information that are collected as part of the patient's clinical care. A Medical Records continuing review form is no longer necessary.

For continuing review of research that is limited to the use of health/medical information on patients. This form may not be used if the study involves an intervention/interaction with patients. This form replaces the Medical Records form.

Research Data Repository
11/06

For continuing review of research limited to establishment of a database of patient information for research purposes. This form replaces the Research-Related Patient Database Form.

For continuing review of research that is limited to the secondary use of human samples and/or data. Secondary use is the use of previously collected samples and/or data for a new research project.