Committee
Meeting Schedule
2007 – 2008 |
August
13, 2008
August 27, 2008
September 10, 2008
September 24, 2008
October 8, 2008
October 22, 2008
November 12, 2008
November 26, 2008
December 10, 2008
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January
14, 2009
January 28, 2009
February 11, 2009
February 25, 2009
March 11, 2009
March 25, 2009
April 8, 2009
April 22, 2009
May 13, 2009
June – TBD
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Human Research
The Institutional Review Board
(IRB) is in place to ensure that human
subjects involved in research are adequately protected and that
the institution
remains in compliance with the regulation. Prior to the initiation
of any research
efforts that involve human subjects the IRB review is required. An IRB Member is assigned as the contact
person for each unit on campus.
This IRB member is available to answer questions and clarify
forms and procedures.
Researchers should submit IRB applications to the ORC. The ORC will process the application and forward it on to the unit's
IRB Contact Member, who
will initiate the review of the proposal.
*Please note:
some items require the Adobe
Acrobat PDF Reader and the Microsoft
Office Viewer both of which can be downloaded
free of charge.
Training
The Office of
Human Research Protections (OHRP), under
the auspices of the Public Health Service, oversees
compliance with the ethical guidelines and regulatory
requirements for research involving human subjects.
The OHRP has published Educational Materials which
may be useful in answering some of the questions that
arise when writing a research protocol.
UNCG's IRB accepts certificates
of training from three sources. Certificates of completion
are available at the end of the tutorial or training
session. This certificate must be printed and attached
to your IRB application.
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Forms
IMPORTANT NOTE:
Approvals for research are valid for a time period established
by the IRB which can't exceed one year. If your research extends
beyond one year, the project must be reviewed and renewed before
the expiration date and prior to continuation. The IRB is directed
by federal guidelines to shut down any and all research using
human participants that does not have a current approval.
IRB Updates - New for 2008-2009 >>Click Here<<
If you have difficulty viewing the files on the page, please contact 6-tech to assist you.
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