SASInstitute A00-282 : Clinical Trials Programming Using SAS 9.4

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SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

1. What is the main focus of 21 CFR Part 11?

A) trial protocol requirements
B) trial safety requirements
C) statistical calculation requirements
D) electronic submission requirements

2. How does the code shown below help to validate report output?
data check;
set datlib.medhist;
mh_len = length(trim(mhcom1));
run;
proc freq data=check;
tables mh_len;
run;

A) It shows all the values for mhcom1 in the results.
B) It writes all values of the mhcom1 variable that are longer than 200 in the results.
C) It shows all the values for the length of mhcom1 in the results.
D) It helps the programmer determine which observation has the longest value for mhcom1.

3. Define.xml is an XML-based submission of a clinical study's:

A) protocol
B) results
C) metadata
D) data

4. Review the following procedure format:

What is the required type of data for the variable in this procedure?

A) Categorical
B) Treatment
C) Character
D) Continuous

5. You are working with the VS data set that contains the variable Pulse.

Which PROC SGPLOT step will produce the graph shown below?

A) proc sgplot data = Work.VS noautolegend;
vbarbasic pulse;
density pulse;
run;
B) proc sgplot data = Work.VS noautolegend;
density pulse;
vbarbasic pulse;
run;
C) proc sgplot data = Work.VS noautolegend;
density pulse;
histogram pulse;
run;
D) proc sgplot data = Work.VS noautolegend;
histogram pulse;
density pulse;
run;

Solutions: