The IRB meets monthly to review proposals received during the previous month. Example: Any proposals submitted in October will be reviewed at the November meeting.
The following pages and links detail the Institutional Review Board for Protection of Human Subjects in Research (IRB). The guidance within applies only to students, faculty, and staff of Bellevue College, Bellevue, WA as researchers or research subjects. The Bellevue College IRB does not review studies that do not involve Bellevue College students, faculty, or staff as either investigators or participants.
Research conducted by Bellevue College affiliates using human participants is overseen by Bellevue College’s IRB. Its purpose is to facilitate human subjects research and to ensure the rights and welfare of human subjects are protected during their participation. To accomplish this purpose, the IRB uses a group process to review research protocols and related materials to ensure the rights and welfare of human subjects are protected.
The IRB reviews and approves all behavioral research activities involving human subjects at Bellevue College through guidelines established for the Code of Federal Regulations established by the Office of Health and Human Services. If you are conducting research, you may not solicit subject participation or begin data collection until your research has received written approval from the IRB. The Bellevue College IRB only reviews projects with direct ties to the Bellevue College community.
The IRB is composed of faculty members, administrators and a member from the community. The human subjects review process is administered through the Office of Effectiveness and Strategic Planning.
Related College Policies and Procedures
- 3650 – Use of Human Participants in Instructional Activities
- 3650P – Use of Human Participants in Instructional Activities Procedures
- 3655 – Use of Human Participants in Research Activities
- 3655P – Use of Human Participants in Research Activities (Procedures)
Related Websites (See Training for additional resources)
The Office for Human Research Protections (OHRP) provides leadership in the protection of the rights, welfare, and wellbeing of subjects involved in research conducted or supported by the U.S. Department of Health and Human Services (HHS). OHRP helps ensure this by providing clarification and guidance, developing educational programs and materials, maintaining regulatory oversight, and providing advice on ethical and regulatory issues in biomedical and social-behavioral research.
The Belmont report attempts to summarize the basic ethical principles identified by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.
Title 45 Public Welfare, Part 46 Protection of Human Subjects
See the section on “Steps to IRB Review” to get started with the application process. This includes determining whether your proposed work requires IRB review and approval.
Questions? Contact: The IRB Chair.