1.24 HRPP Training Requirements for IRB Members

1.0 Purpose

The purpose of this policy and procedure is to describe the Organization’s requirements for training for IRB members and alternates.


2.0 Policy

It is the policy of the Organization that IRB members and alternates will be qualified through initial and continuing education in order to fulfill their responsibility to protect the rights and welfare of human subjects.


3.0 Definitions


4.0 Initial Training and Orientation

  • 4.1. New IRB members, including alternate members, will meet with the IRB Executive Chair or designee, and appropriate IRB Administrators for orientation to cover the following items:
    • 4.1.1. Overview of HHS and FDA regulations
    • 4.1.2. HRPP overview
    • 4.1.3. Structure of IRB meetings
    • 4.1.4. Responsibilities of IRB members
    • 4.1.5. Overview of the Research Support System (RSS).
  • 4.2. New IRB members are provided with the following documents, or a link to those documents on-line, for example, via the UNMC IRB website (http://www.unmc.edu/irb/research-education/regulatory-sites.html).
    • 4.2.1. Belmont Report
    • 4.2.2. Declaration of Helsinki
    • 4.2.3. HHS Regulations at 45 CFR 46
    • 4.2.4. FDA Regulations at 21 CFR 50, 56, 312, 812, 814
    • 4.2.5. Categories of Expedited Review
    • 4.2.6. HRPP policies and procedures
  • 4.3. New IRB members and alternates who also act as investigators or research personnel will be required to complete CITI training (including GCP as appropriate) as per HRPP policy 1.23 (HRPP Training Requirements and Opportunities for Research Personnel). For new IRB members and alternates who do not act as investigators or research personnel, orientation (as described above) will be considered the equivalent of initial CITI training.
  • 4.4. New IRB members are invited to attend an IRB meeting as a guest during the orientation period.
  • 4.5. Full orientation must be completed before the new IRB members may serve as a reviewer or count as a voting member.
  • 4.6. New IRB members are assigned an experienced IRB member as a mentor, to provide assistance as necessary.

5.0 Continuing Education

  • 5.1. Continuing education for IRB members is required throughout service on the IRB in order to ensure ethical oversight of human subject research and compliance with current regulatory and policy requirements.
  • 5.2. IRB members are expected to participate in continuing education which may be obtained through any or all of the following mechanisms:
    • 5.2.1. In-service training at IRB meetings.
    • 5.2.2. Training workshops/webinars.
    • 5.2.3. Regional IRB conferences.
    • 5.2.4. Review of publications distributed by the ORA at IRB meetings or via email.
    • 5.2.5. Review of new information affecting the HRPP such as new laws and regulations, new OHRP/FDA guidance documents, and new or revised HRPP policies distributed by the ORA via email or at IRB meetings.
  • 5.3. Completion of required continuing education will be reviewed with IRB members at the time of their annual evaluation (see HRPP policy 1.22: Assessment of the Effectiveness and Efficiency of the IRB). Members who remain deficient after this review may have their appointment terminated.

6.0 Training Records

The ORA will maintain initial and continuing education training records, and copies of materials distributed to members or presented at IRB meetings. The ORA will maintain all training records for CITI Training by IRB members.


ADMINISTRATIVE APPROVAL: BRUCE G. GORDON, MD IRB EXECUTIVE CHAIR & ASSISTANT VICE CHANCELLOR FOR REGULATORY AFFAIRS CHRISTOPHER KRATOCHVIL, MD INSTITUTIONAL OFFICIAL

POLICY AMENDED:

 REVISED FEBRUARY 1, 2018

 INITIAL DECEMBER 28, 2015