SOCRA CCRP EXAM ACTUAL EXAM 200 QUESTIONS AND CORRECT DETAILED ANSWERS WITH RATIONALES | ALREADY GRADED A+/ BRAND NEW!!!
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Course
SOCRA CCRP
Institution
SOCRA CCRP
SOCRA CCRP EXAM ACTUAL EXAM 200
QUESTIONS AND CORRECT DETAILED
ANSWERS WITH RATIONALES | ALREADY
GRADED A+/ BRAND NEW!!!
What is the federal department responsible for
helping people of Canada maintain and improve
their health? - Answer-Health Canada
.
Who monitors the progress of all c...
protocol required information to be reported to the
sponsor on each trial subject. - Answer-Case Report
Form- CRF
________________ is permission to examine,
analyze, verify, and reproduce any records and
reports that are important to evaluation of a clinical
trial. - Answer-Direct Access
,The form _____________ is used for investigational
new drugs (or IND). - Answer-1571
Under 21CFR312, this form is the statement of the
investigator of a clinical trial. - Answer-1572
What is the FDA form 3455? - Answer-Disclosure
statement for financial disclosure of clinical
investigators who have disclosable interests
The Code of Federal Regulations that applies to
Investigational New Drug Applications is
21CFR_____ - Answer-312
, A sponsor my transfer responsibility for any of all of
the obligations to a _______. - Answer-CRO,
Contract research organization
The clinical investigator will update the financial
disclosure information if any relevant changes occur
during the investigation's course and for _______
following the study's completion. - Answer-one year.
.
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