RC2021 General Course on the IRB Processes and Human Subject Research

Human Subjects Education, Human Subjects Research

RC2022 Single IRB (sIRB) Reliance Agreement for Multi-Site or Collaborative Research

Human Subjects Education, Human Subjects Research

RC2029 Overview of FDA-regulated Research

Human Subjects Education, Human Subjects Research

RC2030 All Things UTRMS-IRB for Single IRB Reliance Studies: Submission, Review, Approval

Human Subjects Education, Human Subjects Research

RC2020 UTRMS Workshop: How to submit a new study, MOD, CR, RNI, and more

Human Subjects Education, Human Subjects Research

RC2024 HRPP Q&A Panel Discussion: All things Human Subject Research

Human Subjects Education, Human Subjects Research

RC2025 HRPP Workshop: Participant Facing Materials

Human Subjects Education, Human Subjects Research

RC2026 Exempt Research Workshop: Complete an Exempt Submission with the IRB

Human Subjects Education, Human Subjects Research

RC2027 Lunch and Learn: When to submit a modification to research, immediate action, and/or continuing review

Human Subjects Education, Human Subjects Research

RC2028 Lunch and Learn: Adverse Events, Unanticipated Problems, and Protocol Deviations

Human Subjects Education, Human Subjects Research