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Reference ICH E6
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Pages with references to ICH E6
Pages in category "Reference ICH E6"
The following 41 pages are in this category, out of 41 total.
C
Certified copy
Clinical study
I
Impartial witness
Independent data-monitoring committee
Independent ethics committee
Informed consent
Institution
Institutional review board
Interim Clinical Trial (Study) Report
Investigational product
Investigator
Investigator's brochure
L
Legally acceptable representative
M
Monitoring
Monitoring report
Multicentre trial
N
Nonclinical study
O
Opinion (in relation to Independent Ethics Committee)
Original medical record
P
Protocol
Protocol Amendment
Q
Quality assurance
Quality control
R
Randomization
Template:Ref-name ich-e6
Regulatory authority
Regulatory inspection
S
Sandbox
Serious adverse event (serious adverse drug reaction)
Source data
Source documents
Sponsor
Sponsor-investigator
Standard operating procedures
Sub-investigator
Subject
Subject identification code
T
Trial site
U
Unexpected adverse drug reaction
V
Vulnerable subjects
W
Well-being
