OPRS SOP 906: Protection Of Research Participants
Approved Date
Revised Date
Full Details
POLICY
It is the policy of the University of Illinois Urbana-Champaign IRB that before an administrative hold, suspension, or termination is put into effect, the convened IRB or IRB designee considers whether any additional procedures need to be followed to protect the rights and welfare of current participants.
In this policy, an IRB designee refers to the following: The IRB Chair, IRB Vice-Chair, OPRS Director, Institutional Official, or a person designated in writing to temporarily assume the role of one of those persons.
PROCEDURES
1. The IRB requires the Investigator to submit proposed procedures for withdrawal of currently enrolled subjects that considers their rights and welfare. The convened IRB or IRB designee reviews the proposed procedures. These procedures may include but are not limited to:
· Submitting a list of all currently enrolled participants including their status within the study;
- Transferring participants to another investigator;
- Making arrangements for clinical care outside the research;
· Allowing continuation of some research activities under the supervision of an independent monitor; or
· Requiring or permitting follow-up of participants for safety reasons.
The convened IRB or IRB designee may approve or request changes to the proposed procedures for withdrawal of enrolled subjects.
2. The IRB requires the Investigator to submit a proposed script or letter notifying all currently enrolled and former participants that are affected by the administrative hold, suspension, or termination. The convened IRB or IRB designee reviews the proposed script or letter and may approve or request changes to the proposed script or letter.
3. If follow-up of subjects for safety reasons is permitted/required by the IRB, participants should be so informed, and any unanticipated problems involving risks to participants or others must be reported to the IRB and others as required by the protocol and organizational policies and procedures.
4. The IRB may mandate oversight or transfer responsibility to another investigator to assure implementation of the above procedures.