Links and Resources
- Blood Draws
- Chart or Record Reviews
- CLIA Certification
- ClinicalTrials.gov Registration & Reporting Requirements
- Consent
- Data Security
- Deception
- Department of Defense
- Drugs, Biologics, and Dietary Supplements
- Exercise Testing
- Glossary of Research Related Terms
- Graduate School Policy on IRB Approval
- International Research
- Letters of Support from External Sites of Recruitment or Research
- Medical Devices
- Public Schools
- Race and Ethnicity
- Recruitment of Research Participants
- Snowball Sampling
- Students and Employees as Research Participants
- Tribal Populations
Determining your data security level
Engagement in research decision tree
FDA
Medical Devices
- Is it a medical device?
- Can it be exempt from the requirements for an IDE application?
- Is it significant risk or nonsignificant risk?
Does FERPA apply to my human subject research study?
When do you need parental permission for research with children?
Does the Protection of Pupil's Rights Amendment (PPRA) apply to my research study?
- Common Rule 45 CFR 46 (OHRP)
- Protection of Human Subjects 21 CFR 50 (FDA)
- Institutional Review Boards 21 CFR 56 (FDA)
- 10 CFR 745 US Department of Energy
- 21 CFR 50 US Food and Drug Administration
- 34 CFR 97 US Department of Education
- 34 CFR 98 US Department of Education (PPRP)
- 34 CFR 99 US Department of Education (FERPA)
- 45 CFR 46 US Department of Health and Human Services
- Office for Human Research Protections (OHRP)
- DHHS Policy for IRB Review of Applications for HHS Support
- HIPAA
- Data and Safety Monitoring (NIDDK)
- NIH Policy for IRB Review of Human Subjects Protocols in Grant Applications
- Investigator Responsibilities (OHRP)
- Recruitment Strategies: Adults in Behavioral Studies (University of WA ITHS)
- Inclusion of Women and Minorities (NIH)
- International Compilation of Human Subject Research Protections (OHRP)
- ClinicalTrials.gov
- IRB Fact Sheet: Oregon's Genetic Privacy Law (Oregon DHS)
The policies and guidance put forth by the OSU Human Research Protection Program borrow extensively from the best practices of a variety of academic institutions, reflect the advice received from federal regulators, and are informed by input from leaders in research ethics. The information in these guidance documents builds on ideas freely shared between institutions and exists because of the generosity and collegiality demonstrated by the community of professionals who work in the field of human research protections.