IRB Approvals

Attachments 4A-4C - IRB Approvals.doc

Generic Clearance to Collect Medical Outcome and Risk Factor Data from a Cohort of U.S. Radiologic Technologists

IRB Approvals

OMB: 0925-0405

Document [doc]
Download: doc | pdf

A ttachment 4A – National Cancer Institute IRB Approval (OH97-C-N053)

Attachment 4B – University of Minnesota IRB – Main Study (8005M02489)


Subject:

IRB Approval of Continuing Review

From:

[email protected]

Date:

Fri, 15 Sep 2006 23:10:08 -0500 (CDT)

To:

[email protected]


The IRB: Human Subjects Committee renewed its approval of the referenced study listed below:


Study Number: 8005M02489


Principal Investigator: Bruce Alexander


Expiration Date: 09/13/2007


Approval Date: 09/14/2006


Title(s):

Cancer Risk in X-Ray Technologists


U.S. Radiologic Technologists Cohort: New Strategies for Follow-up


The U.S. Radiologic Technologists Study

________________________________________________________


You may go to the View Completed section of http://eresearch.umn.edu/ to view or print your continuing review submission.


For grant certification purposes you will need this date and the Assurance of Compliance number, which is FWA00000312 (Fairview Health Systems Research FWA00000325, Gillette Childrens Specialty Healthcare FWA00004003). Approval will expire one year from that date. You will receive a report form two months before the expiration date.


In the event that you submitted a consent document with the continuing review form, it has also been reviewed and approved. If you provided a summary of subjects' experience to include non-UPIRTSO events, these are hereby acknowledged.


As Principal Investigator of this project, you are required by federal regulations to inform the IRB of any proposed changes in your research that will affect human subjects. Changes should not be initiated until written IRB approval is received. Unanticipated problems and adverse events should be reported to the IRB as they occur. Research projects are subject to continuing review.


If you have any questions, please call the IRB office at (612) 626-5654.


The IRB wishes you continuing success with your research.

Attachment 4C – University of Minnesota IRB – Genetic Studies (9312M07534)


Subject:

IRB Approval of Continuing Review

From:

[email protected]

Date:

Thu, 5 Oct 2006 23:10:11 -0500 (CDT)

To:

[email protected]


The IRB: Human Subjects Committee renewed its approval of the referenced study listed below:


Study Number: 9312M07534


Principal Investigator: Bruce Alexander


Expiration Date: 10/03/2007


Approval Date: 10/04/2006


Title(s):

Cancer Risks in X-Ray Technologists: Early-Onset Breast Cancer among Radiation Technologists


Genetics Studies among Radiologic Technologists

________________________________________________________


This e-mail confirmation is your official University of Minnesota RSPP notification of continuing review approval. You will not receive a hard copy or letter.

This secure electronic notification between password protected authentications has been deemed by the University of Minnesota to constitute a legal signature.


You may go to the View Completed section of http://eresearch.umn.edu/ to view or print your continuing review submission.


For grant certification purposes you will need this date and the Assurance of Compliance number, which is FWA00000312 (Fairview Health Systems Research FWA00000325, Gillette Childrens Specialty Healthcare FWA00004003). Approval will expire one year from that date. You will receive a report form two months before the expiration date.


In the event that you submitted a consent document with the continuing review form, it has also been reviewed and approved. If you provided a summary of subjects' experience to include non-UPIRTSO events, these are hereby acknowledged.


As Principal Investigator of this project, you are required by federal regulations to inform the IRB of any proposed changes in your research that will affect human subjects. Changes should not be initiated until written IRB approval is received. Unanticipated problems and adverse events should be reported to the IRB as they occur. Research projects are subject to continuing review.


If you have any questions, please call the IRB office at (612) 626-5654.


The IRB wishes you continuing success with your research.

File Typeapplication/msword
File TitleAttachment 6A – National Cancer Institute IRB Approval (OH97-C-N053)
AuthorMichelle Doody
Last Modified Byanisz
File Modified2007-03-01
File Created2007-03-01

© 2024 OMB.report | Privacy Policy