- Who We Are
- Clinician Employment
- Publications
- Witness to Witness (W2W)
- El Premio Kugel & Zuroweste a la Justicia en la Salud
- Your Voice Matters: Photovoice Project
Ethics in Research: Protecting Human Subjects
National Farmworker Health Conference (May 22) - Presentation
Files
CITI - Collaborative IRB Training Initiative
Completion of the web-based education course is required for all investigators and research team members, regardless of the source or type of funding.
Recertification is required every 3 years after initial certification. Researchers must take the Basic Course for your Learner Group for recertification. After this, you are only required to complete the Refresher Course for recertification. Recertification is required every 3 years.
Guidelines for informed consent
Files
-
- A-Guidelines for informed consent- ( 50 Kb )
-
- A-Guidelines for informed consent ( 63 Kb )
HIPPA Compliance
Files
-
- A-HIPPA Compliance application ( 92 Kb )
-
- A-HIPPA Compliance application ( 188 Kb )
Initial Protocol Review Form
Files
-
- A-Initial protocol review form ( 42 Kb )
-
- A-Initial protocol review form ( 57 Kb )
Protocols with minors as participants
Files
-
- A-Protocols with minors as participants ( 34 Kb )
-
- A-Protocols with minors as participants ( 29 Kb )
The Belmont Report
The Belmont Report is a report created by the former United States Department of Health, Education, and Welfare (which was renamed to Health and Human Services) entitled "Ethical Principles and Guidelines for the Protection of Human Subjects of Research" and is an important historical document in the field of medical ethics. The report was created on April 18, 1979 and gets its name from the Belmont Conference Center where the document was drafted.
Files
-
- The Belmont Report ( 63 Kb )
