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Protocols already approved
by IRB must be submitted at least one time per
year for renewal purposes. At that time the
following information must be addressed:
-
Number of subjects
-
Description - any
adverse event or problems-How many subjects
withdraw
-
Summary of any
recent literature since last approval
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A copy of the
currently informed consent form
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Fill out the
“Continuing Review Form”
Also, we would like to
remind all faculty and laboratory personnel
dealing with protocols involving human subjects
that they must take training courses available
at
http://phrp.nihtraining.com, and
http://irb.ucsd.edu/hipaatutorial/login.html
for all investigators and key personnel.
Training certificates are valid for three years.
Download Continuing review form
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