A
·
B
·
C
·
D
·
E
·
F
·
G
·
H
·
I
·
J
·
K
·
L
·
M
·
N
·
O
·
P
·
Q
·
R
·
S
·
T
·
U
·
V
·
W
·
X
·
Y
·
Z
·
OTHER
·

Directory Results for The IRB is responsible to review reported protocol violations involving human subjects and may request appropriate measures be taken to rectify the violation to ensure that the violation does not reoccur to The IRB may approve an oral consent process (see 45 CFR 46

The IRB is responsible to review reported protocol violations involving human subjects and may request appropriate measures be taken to rectify the violation to ensure that the violation does not reoccur
The IRB mandates that all adverse events be reported as soon as possible (but no later than 5 working days after the event)
The IRB may approve an oral consent process (see 45 CFR 46