Committee
Meeting Schedule
2009 – 2010 |
August
12, 2009
August 26, 2009
September 9, 2009
September 23, 2009
October 7, 2009
October 21, 2009
November 4, 2009
November 18, 2009
December 2, 2009
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January 20, 2010
February 3, 2010
February 17, 2010
March 3, 2010
March 17, 2010
April 7, 2010
April 21, 2010
May 5, 2010
May 19, 2010
June TBA
July TBA
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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. Researchers should submit IRB applications to the ORC.
*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 2009-2010 >>Click Here<<
If you have difficulty viewing the files on the page, please contact 6-tech to assist you.
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