IRB Approval Document

APPROVAL
February 9, 2022
Youn Lee
919-541-8735, x28735
younlee@rti.org
Dear Youn Lee:
On 2/9/2022, the IRB reviewed the following submission:
Type of Review:
Title:
Investigator:
IRB ID:
Funding Source:
Customer/Client Name:
Project/Proposal Number:
Contract/Grant Number:
IND, IDE, or HDE:

Initial Study
Nicotine Education Project
Youn Lee
STUDY00021856
FDA CFSAN
FDA CFSAN
0214634.027.000
HHSF223201510002B
None

The IRB approved the study on 2/9/2022. Any changes to the approved study protcol or
documents must be submitted to the IRB as a modification for review and approval prior
to implementation. Within 30 days of study completion, you should request to close the
study in IRB Express. You can submit a modification or study closure by navigating to
the active study and clicking Create Modification / CR.
In conducting this protocol, you are required to follow the requirements listed in the
Investigator Manual (HRP-103), which can be found by navigating to the IRB Library
within the IRB system.
Sincerely,
The RTI Office of Research Protection

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