Form 2 IRB Certification

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Attachment_A02_irbcrt-102221_Clean

CTSU IRB Certification Form (Attachment A2)

OMB: 0925-0753

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Attachment_A02_IRB Certification

OMB# 0925-0753

Expiration Date 05/31/2024



Public reporting burden for this collection of information is estimated to average 10 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to: NIH, Project Clearance Branch, 6705 Rockledge Drive, MSC 7974, Bethesda, MD 20892-7974, ATTN: PRA (OMB#0925-0753). Do not return the completed form to this address.

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Cancer Trials Support Unit INSTITUTIONAL REVIEW BOARD CERTIFICATION


Submit to the CTSU Regulatory Office via the Regulatory Submission Portal: www.ctsu.org.

1) Protocol #: (Lead Group #)

2) Protocol Version:

3) Protocol Title:

4) Institution Name (List all institutions covered by IRB approval that will conduct this study. Attach supplemental list if necessary.)

Indicate # sites on supplemental sheet if applicable:

5) NCI Institution Code





6) Principal Investigator:

7) NCI Investigator #:

This activity has been reviewed and approved by the IRB in accordance with the Common Rule and any other governing regulations or

subparts:

8) Approval Type:


Original Amendment Renewal

9) Review Type:


Full Board Expedited*

*Provide OHRP Expedited Review Category in Box 10

10) Expedited Review Categories (Pick only one for Box #9):

(45CFR46.110.8a-c: Continuing review of research previously approved by a convened IRB)

8.a Where (i) the research is permanently closed to the enrollment of new subjects; (ii) all subjects have completed all research- related

interventions; and (iii) the research remains active only for long-term follow-up of subjects

8.b Where no subjects have been enrolled and no additional risks have been identified

8.c Where the remaining research activities are limited to data analysis


10a) Other Expedited Review Categories outlined on OHRP's website:

11) Date of IRB or Designee Review from box 9:

12) Approval Period: Effective Date must be on or after box 11 date and on or after box 13 date, if applicable.

Effective: Expiration:

13) Was the protocol approved with contingencies? YES NO Provide date all contingencies were

approved by the IRB or Designee:

15) Comments:

14) OHRP IRB Registration Number (8 digits long): IRB

The official signing below certifies that the information provided above is correct and that, as required, future reviews will be performed & certification will be provided. Questions #1 through #20 must be completed for this form to be accepted.

16) Name of IRB Signatory:

17) Name of approving IRB:

18) Title of IRB Signatory:

19) Phone:

20) Signature:

21) Date:


Cancer Trials Support Unit INSTITUTIONAL REVIEW BOARD CERTIFICATION


Submit to the CTSU Regulatory Office via the Regulatory Submission Portal: www.ctsu.org.

In Reference to Protocol #:

Additional Institution Names (List all additional institutions covered

by IRB approval that will conduct this study.)

NCI Institution

Code

Ex. University of Texas

TX002

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5)


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7)


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File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
File TitleCTSU INSTITUTIONAL REVIEW BOARD CERTIFICATION
SubjectCTSU INSTITUTIONAL REVIEW BOARD CERTIFICATION
AuthorDemetrius Williams
File Modified0000-00-00
File Created2022-09-08

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