Required Training
Federal law, Kaiser Permanente's (KP) Federal-wide Assurance (FWA) agreement with the Office of Human Subjects Research Protection (OHRP), and KP policy require each person who participates in the design and conduct of human subjects research studies, including the investigator, IRB, or KP research support staff, to obtain KP's required training prior to conducting research.
- Privacy/Security/Confidentiality Training for KP Researchers
- Human Research Participant Protection Training
Additionally, for Health Services Research Teams
- Reporting Protocol Violations, Deviations, and Exemption
- Reporting of Adverse Events and Other Safety Information (if applicable)
Additionally, for Clinical Trials Research Teams
- Conducting FDA-Regulated Clinical Trials in KP
- Reporting Protocol Violations, Deviations, and Exemption
- Reporting of Adverse Events and Other Safety Information
- Humanitarian Use Devices (if implanting OR providing devices)
- International Air Transportation Agency/Dept of Transportation (IATA/DOT) Training Certification
- Investigational Drug Accountability and Management